NM_000083.3(CLCN1):c.2059G>C (p.Asp687His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003145009.3
Allele description [Variation Report for NM_000083.3(CLCN1):c.2059G>C (p.Asp687His)]
NM_000083.3(CLCN1):c.2059G>C (p.Asp687His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024