Allele Registry

Canonical Allele Identifier: PA658832682

Gene: DPYD HGNC NCBI

ClinVar Allele:

541381

ClinVar RCV:

RCV000669112

RCV002531218

ClinVar Variation:

553625

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153773.1:p.Lys63Glu	CA963770 NM_001160301.1:c.187A>G