NM_000083.3(CLCN1):c.651C>T (p.Val217=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 17, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000441602.4
Allele description [Variation Report for NM_000083.3(CLCN1):c.651C>T (p.Val217=)]
NM_000083.3(CLCN1):c.651C>T (p.Val217=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 5, 2024