NM_004366.6(CLCN2):c.2156C>T (p.Ser719Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002487039.1
Allele description [Variation Report for NM_004366.6(CLCN2):c.2156C>T (p.Ser719Leu)]
NM_004366.6(CLCN2):c.2156C>T (p.Ser719Leu)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023