Canonical Allele Identifier: PA2829310367
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387574.1:p.Cys247Arg
CA350294001
NM_001400645.1:c.739T>C