Allele Registry

Canonical Allele Identifier: PA2830111913

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004120196

ClinVar Variation:

2263887

HGVS (amino-acid)	Matching Registered Transcripts
NP_127463.2:p.Gln316His	CA614336 NM_032996.3:c.948G>T CA338562534 NM_032996.3:c.948G>C