Allele Registry

Canonical Allele Identifier: PA2826281306

Gene: CASP8 HGNC NCBI

ClinVar Allele:

1453274

ClinVar RCV:

RCV002033008

ClinVar Variation:

1347161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001219.2:p.Asp302Asn	CA350298761 NM_001228.4:c.904G>A