NM_004366.6(CLCN2):c.2410C>T (p.His804Tyr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002904539.2
Allele description [Variation Report for NM_004366.6(CLCN2):c.2410C>T (p.His804Tyr)]
NM_004366.6(CLCN2):c.2410C>T (p.His804Tyr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024