Allele Registry

Canonical Allele Identifier: PA200994

Gene: DPYD HGNC NCBI

ClinVar Allele:

105969

ClinVar RCV:

RCV000086475

RCV000174446

RCV000389596

RCV001787907

RCV001787908

RCV003891586

ClinVar Variation:

100092

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Ile543Val	CA200992 NM_000110.4:c.1627A>G