Allele Registry

Canonical Allele Identifier: PA102083

Gene: DPYD HGNC NCBI

ClinVar RCV:

RCV000000466

RCV002281683

ClinVar Variation:

437

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Arg886His	CA114282 NM_000110.4:c.2657G>A