Canonical Allele Identifier: PA2580251790
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387608.1:p.Leu214Pro
CA350294001
NM_001400679.1:c.641T>C