Allele Registry

Canonical Allele Identifier: PA2826575917

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004158617

ClinVar Variation:

2312361

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264983.1:p.Met250Ile	CA338562525 NM_001278054.2:c.750G>T CA338562526 NM_001278054.2:c.750G>C CA338562527 NM_001278054.2:c.750G>A