Canonical Allele Identifier: PA2829312013
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387587.1:p.Cys221Arg
CA350294001
NM_001400658.1:c.661T>C