Allele Registry

Canonical Allele Identifier: PA2826281401

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004311714

RCV004429972

ClinVar Variation:

2540333

3137660

HGVS (amino-acid)	Matching Registered Transcripts
NP_001220.2:p.Met39Ile	CA614734 NM_001229.5:c.117G>A CA338570948 NM_001229.5:c.117G>T CA338570950 NM_001229.5:c.117G>C