Allele Registry

Canonical Allele Identifier: PA2829314766

Gene: CASP8 HGNC NCBI

ClinVar Allele:

1453274

ClinVar RCV:

RCV002033008

ClinVar Variation:

1347161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387605.1:p.Asp71Asn	CA350298761 NM_001400676.1:c.211G>A