Allele Registry

Canonical Allele Identifier: PA228099

Gene: DPYD HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

105957

ClinVar RCV:

RCV000086462

RCV000249656

RCV000407597

RCV001787902

RCV001787903

RCV001787904

RCV003891585

ClinVar Variation:

100080

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Val732Ile	CA228097 NM_000110.4:c.2194G>A