NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Nov 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000419685.4
Allele description
NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu)
Condition(s)
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jun 15, 2021