Canonical Allele Identifier: PA2741838479
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 2606986
ClinVar RCV Id: RCV003355047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153773.1:p.Arg70Gln
CA963766
NM_001160301.1:c.209G>A