Canonical Allele Identifier: PA2829314344
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387602.1:p.Cys37Arg
CA350294001
NM_001400673.1:c.109T>C