NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu) AND CHRNA2-related condition
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 12, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003905194.1
Allele description [Variation Report for NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu)]
NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu)
Condition(s)
- Name:
- CHRNA2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 1, 2024