Canonical Allele Identifier: PA2580167605
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 1787404
ClinVar RCV Id: RCV002425548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153773.1:p.Leu73Arg
CA963765
NM_001160301.1:c.218T>G