Allele Registry

Canonical Allele Identifier: PA658825252

Gene: DPYD HGNC NCBI

ClinVar RCV:

RCV000666781

ClinVar Variation:

551659

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Lys958Glu	CA962914 NM_000110.4:c.2872A>G