Canonical Allele Identifier: PA2830106254
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203519.1:p.Gly234Glu
CA350293942
NM_033355.3:c.701G>A