Canonical Allele Identifier: PA2829314220
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387601.1:p.Gly35Glu
CA350293942
NM_001400672.1:c.104G>A