NM_000052.7(ATP7A):c.1737A>G (p.Val579=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 24, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000418443.1
Allele description
NM_000052.7(ATP7A):c.1737A>G (p.Val579=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 15, 2021