Na+/K+ transporting ATPase alpha 2 polypeptide, partial [Homo sapiens]

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The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients. [Brain Dev. 2023]
The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients.
Dai L, Ding C, Tian X, Liu M, Ma Y, Chen C, Ren X, Li H. Brain Dev. 2023 Sep; 45(8):422-431. Epub 2023 May 2.
Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases. [Neurosci Res. 2022]
Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases.
Oda I, Danno D, Saigoh K, Wolf J, Kawashita N, Hirano M, Samukawa M, Kitamura S, Kikui S, Takeshima T, et al. Neurosci Res. 2022 Jul; 180:83-89. Epub 2022 Mar 4.
Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms. [J Headache Pain. 2021]
Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.
Li Y, Tang W, Kang L, Kong S, Dong Z, Zhao D, Liu R, Yu S. J Headache Pain. 2021 Aug 12; 22(1):92. Epub 2021 Aug 12.

RefSeq genomic sequence
See the genomic reference sequence for the ATP1A2 gene (NG_008014.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the ATP1A2 gene.

Nucleotide
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