Canonical Allele Identifier: PA915967791
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073594.1:p.Gly293Glu
CA350293942
NM_001080125.1:c.878G>A