Allele Registry

Canonical Allele Identifier: PA2580171285

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004120196

ClinVar Variation:

2263887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001220.2:p.Gln399His	CA614336 NM_001229.5:c.1197G>T CA338562534 NM_001229.5:c.1197G>C