Canonical Allele Identifier: PA119054
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203519.1:p.Asp285His
CA119051
NM_033355.3:c.853G>C