Allele Registry

Canonical Allele Identifier: PA2830106500

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV002033008

ClinVar Variation:

1347161

HGVS (amino-acid)	Matching Registered Transcripts
NP_203520.1:p.Asp270Asn	CA350298761 NM_033356.4:c.808G>A