NM_001289808.2(CRYAB):c.60C>T (p.Pro20=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001528828.2
Allele description [Variation Report for NM_001289808.2(CRYAB):c.60C>T (p.Pro20=)]
NM_001289808.2(CRYAB):c.60C>T (p.Pro20=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 6, 2024