Canonical Allele Identifier: PA2829312036
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387587.1:p.Asp270His
CA119051
NM_001400658.1:c.808G>C