Canonical Allele Identifier: PA2825950017
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 3085641
ClinVar RCV Id: RCV004376961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153773.1:p.Asp61His
CA341379475
NM_001160301.1:c.181G>C