Allele Registry

Canonical Allele Identifier: PA2580171275

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004155509

ClinVar Variation:

2308169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001220.2:p.Ser307Tyr	CA614426 NM_001229.5:c.920C>A