Allele Registry

Canonical Allele Identifier: PA658825239

Gene: DPYD HGNC NCBI

ClinVar Allele:

541411

ClinVar RCV:

RCV000665570

ClinVar Variation:

550741

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Asp342Asn	CA963459 NM_000110.4:c.1024G>A