Allele Registry

Canonical Allele Identifier: PA913191611

Gene: DPYD HGNC NCBI

ClinVar Allele:

623098

ClinVar RCV:

RCV000786704

RCV003479218

ClinVar Variation:

635267

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Val995Phe	CA27458647 NM_000110.4:c.2983G>T