Allele Registry

Canonical Allele Identifier: PA2830111901

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004335097

ClinVar Variation:

2592219

HGVS (amino-acid)	Matching Registered Transcripts
NP_127463.2:p.Leu192Met	CA614453 NM_032996.3:c.574C>A