Allele Registry

Canonical Allele Identifier: PA119049

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV000008201

ClinVar Variation:

7760

HGVS (amino-acid)	Matching Registered Transcripts
NP_001219.2:p.Arg265Trp	CA119046 NM_001228.4:c.793C>T