Allele Registry

Canonical Allele Identifier: PA2829310395

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV000640975

ClinVar Variation:

533732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387574.1:p.Ile309Val	CA2053716 NM_001400645.1:c.925A>G