NM_002617.4(PEX10):c.*173G>A AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001689976.1
Allele description [Variation Report for NM_002617.4(PEX10):c.*173G>A]
NM_002617.4(PEX10):c.*173G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Hyperinsulinism-hyperammonemia syndrome
Hyperinsulinism-hyperammonemia syndromeMedGen
-
C1847555[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023