Canonical Allele Identifier: PA2825464602
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073593.1:p.Gly219Glu
CA350293942
NM_001080124.1:c.656G>A