NM_000388.4(CASR):c.762T>C (p.His254=) AND Familial hypocalciuric hypercalcemia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000404951.12
Allele description [Variation Report for NM_000388.4(CASR):c.762T>C (p.His254=)]
NM_000388.4(CASR):c.762T>C (p.His254=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024