Canonical Allele Identifier: PA2825464763
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073594.1:p.Cys295Arg
CA350294001
NM_001080125.1:c.883T>C