Allele Registry

Canonical Allele Identifier: PA2830111906

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004259782

ClinVar Variation:

2472216

HGVS (amino-acid)	Matching Registered Transcripts
NP_127463.2:p.Ile258Thr	CA614408 NM_032996.3:c.773T>C