Allele Registry

Canonical Allele Identifier: PA2829311639

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV000008201

ClinVar Variation:

7760

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387585.1:p.Arg248Trp	CA119046 NM_001400656.1:c.742C>T