Allele Registry

Canonical Allele Identifier: PA645486266

Gene: DPYD HGNC NCBI

ClinVar Allele:

267156

ClinVar RCV:

RCV000280781

RCV001004163

RCV001788185

RCV001788186

RCV002282099

ClinVar Variation:

282919

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Arg592Trp	CA963238 NM_000110.4:c.1774C>T