Allele Registry

Canonical Allele Identifier: PA645486233

Gene: DPYD HGNC NCBI

ClinVar RCV:

RCV000393255

ClinVar Variation:

298293

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Ser492Leu	CA963340 NM_000110.4:c.1475C>T