Allele Registry

Canonical Allele Identifier: PA2830111914

Gene: CASP9 HGNC NCBI

ClinVar RCV:

RCV004158617

ClinVar Variation:

2312361

HGVS (amino-acid)	Matching Registered Transcripts
NP_127463.2:p.Met317Ile	CA338562525 NM_032996.3:c.951G>T CA338562526 NM_032996.3:c.951G>C CA338562527 NM_032996.3:c.951G>A