NM_000388.4(CASR):c.2692C>T (p.Arg898Trp) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001966167.5
Allele description [Variation Report for NM_000388.4(CASR):c.2692C>T (p.Arg898Trp)]
NM_000388.4(CASR):c.2692C>T (p.Arg898Trp)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024