Allele Registry

Canonical Allele Identifier: PA2826575910

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004259782

ClinVar Variation:

2472216

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264983.1:p.Ile191Thr	CA614408 NM_001278054.2:c.572T>C