NM_000053.4(ATP7B):c.3416C>G (p.Ala1139Gly) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001579789.3
Allele description [Variation Report for NM_000053.4(ATP7B):c.3416C>G (p.Ala1139Gly)]
NM_000053.4(ATP7B):c.3416C>G (p.Ala1139Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024