NM_000053.4(ATP7B):c.1023C>T (p.Ser341=) AND Wilson disease
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001443615.13
Allele description [Variation Report for NM_000053.4(ATP7B):c.1023C>T (p.Ser341=)]
NM_000053.4(ATP7B):c.1023C>T (p.Ser341=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024