Allele Registry

Canonical Allele Identifier: PA2830111904

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004155509

ClinVar Variation:

2308169

HGVS (amino-acid)	Matching Registered Transcripts
NP_127463.2:p.Ser224Tyr	CA614426 NM_032996.3:c.671C>A