Canonical Allele Identifier: PA2580251817
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387679.1:p.Asp86His
CA119051
NM_001400750.1:c.256G>C