Allele Registry

Canonical Allele Identifier: PA228161

Gene: DPYD HGNC NCBI

ClinVar Allele:

105990

ClinVar RCV:

RCV000086496

RCV000671354

RCV001787913

RCV001787914

RCV002222386

RCV003964961

ClinVar Variation:

100113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Tyr186Cys	CA228159 NM_000110.4:c.557A>G