Canonical Allele Identifier: PA2829313879
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387598.1:p.Cys133Arg
CA350294001
NM_001400669.1:c.397T>C