Allele Registry

Canonical Allele Identifier: PA2741809241

Gene: DPYD HGNC NCBI

ClinVar Allele:

2834176

ClinVar RCV:

RCV003466229

ClinVar Variation:

2674903

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Ser201Arg	CA963612 NM_000110.4:c.601A>C CA341379732 NM_000110.4:c.603T>G CA341379733 NM_000110.4:c.603T>A