Allele Registry

Canonical Allele Identifier: PA2829313611

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV002033008

ClinVar Variation:

1347161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387596.1:p.Asp201Asn	CA350298761 NM_001400667.1:c.601G>A