Allele Registry

Canonical Allele Identifier: PA2829313304

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV000640975

ClinVar Variation:

533732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387594.1:p.Ile273Val	CA2053716 NM_001400665.1:c.817A>G