NM_000053.4(ATP7B):c.3226A>G (p.Thr1076Ala) AND Wilson disease
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004011962.2
Allele description [Variation Report for NM_000053.4(ATP7B):c.3226A>G (p.Thr1076Ala)]
NM_000053.4(ATP7B):c.3226A>G (p.Thr1076Ala)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024