Allele Registry

Canonical Allele Identifier: PA228170

Gene: DPYD HGNC NCBI

ClinVar Allele:

105993

ClinVar RCV:

RCV000086499

RCV000245015

RCV000276917

RCV001787915

RCV001787916

RCV003891588

ClinVar Variation:

100116

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Met166Val	CA228168 NM_000110.4:c.496A>G