Allele Registry

Canonical Allele Identifier: PA915986205

Gene: DPYD HGNC NCBI

ClinVar RCV:

RCV000991926

RCV002488088

ClinVar Variation:

804763

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153773.1:p.Pro92Ala	CA963742 NM_001160301.1:c.274C>G