Allele Registry

Canonical Allele Identifier: PA2580171281

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004259782

ClinVar Variation:

2472216

HGVS (amino-acid)	Matching Registered Transcripts
NP_001220.2:p.Ile341Thr	CA614408 NM_001229.5:c.1022T>C