NM_000053.4(ATP7B):c.1296T>A (p.Ser432=) AND Wilson disease
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Nov 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003504348.3
Allele description [Variation Report for NM_000053.4(ATP7B):c.1296T>A (p.Ser432=)]
NM_000053.4(ATP7B):c.1296T>A (p.Ser432=)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024