Canonical Allele Identifier: PA119055
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001219.2:p.Asp302His
CA119051
NM_001228.4:c.904G>C