NM_000053.4(ATP7B):c.1298C>G (p.Thr433Ser) AND Wilson disease
- Germline classification:
- Uncertain significance (4 submissions)
- Last evaluated:
- Sep 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001277083.7
Allele description [Variation Report for NM_000053.4(ATP7B):c.1298C>G (p.Thr433Ser)]
NM_000053.4(ATP7B):c.1298C>G (p.Thr433Ser)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024