NM_000053.4(ATP7B):c.*1182C>T AND Wilson disease
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000262520.5
Allele description [Variation Report for NM_000053.4(ATP7B):c.*1182C>T]
NM_000053.4(ATP7B):c.*1182C>T
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023