Allele Registry

Canonical Allele Identifier: PA2826575908

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004155509

ClinVar Variation:

2308169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264983.1:p.Ser157Tyr	CA614426 NM_001278054.2:c.470C>A