NM_000053.4(ATP7B):c.*1782C>G AND Wilson disease
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000336343.7
Allele description [Variation Report for NM_000053.4(ATP7B):c.*1782C>G]
NM_000053.4(ATP7B):c.*1782C>G
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024