Allele Registry

Canonical Allele Identifier: PA102071

Gene: DPYD HGNC NCBI

ClinVar RCV:

RCV000362597

RCV000786703

ClinVar Variation:

298300

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Arg235Trp	CA963582 NM_000110.4:c.703C>T