Allele Registry

Canonical Allele Identifier: PA2741841076

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004335097

ClinVar Variation:

2592219

HGVS (amino-acid)	Matching Registered Transcripts
NP_001220.2:p.Leu275Met	CA614453 NM_001229.5:c.823C>A