NM_000053.4(ATP7B):c.2681C>G (p.Thr894Ser) AND Wilson disease
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004016982.2
Allele description [Variation Report for NM_000053.4(ATP7B):c.2681C>G (p.Thr894Ser)]
NM_000053.4(ATP7B):c.2681C>G (p.Thr894Ser)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024