NM_000388.4(CASR):c.402C>T (p.His134=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003790839.1
Allele description [Variation Report for NM_000388.4(CASR):c.402C>T (p.His134=)]
NM_000388.4(CASR):c.402C>T (p.His134=)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024