Allele Registry

Canonical Allele Identifier: PA2826575916

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004120196

ClinVar Variation:

2263887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264983.1:p.Gln249His	CA614336 NM_001278054.2:c.747G>T CA338562534 NM_001278054.2:c.747G>C