Canonical Allele Identifier: PA2826281281
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001219.2:p.Gly251Glu
CA350293942
NM_001228.4:c.752G>A