Allele Registry

Canonical Allele Identifier: PA2829313902

Gene: CASP8 HGNC NCBI

ClinVar Allele:

1453274

ClinVar RCV:

RCV002033008

ClinVar Variation:

1347161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387598.1:p.Asp182Asn	CA350298761 NM_001400669.1:c.544G>A