NM_000053.4(ATP7B):c.747G>A (p.Leu249=) AND Wilson disease
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000982754.11
Allele description [Variation Report for NM_000053.4(ATP7B):c.747G>A (p.Leu249=)]
NM_000053.4(ATP7B):c.747G>A (p.Leu249=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024