Canonical Allele Identifier: PA2829313129
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387593.1:p.Cys213Arg
CA350294001
NM_001400664.1:c.637T>C