NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Mar 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000124278.3
Allele description
NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 29, 2021