Allele Registry

Canonical Allele Identifier: PA102097

Gene: DPYD HGNC NCBI

ClinVar RCV:

RCV000000464

RCV000711510

RCV001787362

RCV001787363

RCV002247229

ClinVar Variation:

435

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Cys29Arg	CA114278 NM_000110.4:c.85T>C