Allele Registry

Canonical Allele Identifier: PA2580171288

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004158617

ClinVar Variation:

2312361

HGVS (amino-acid)	Matching Registered Transcripts
NP_001220.2:p.Met400Ile	CA338562525 NM_001229.5:c.1200G>T CA338562526 NM_001229.5:c.1200G>C CA338562527 NM_001229.5:c.1200G>A