Allele Registry

Canonical Allele Identifier: PA2829314381

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV000640975

ClinVar Variation:

533732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387602.1:p.Ile99Val	CA2053716 NM_001400673.1:c.295A>G