Canonical Allele Identifier: PA2825075196
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 1787404
ClinVar RCV Id: RCV002425548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Leu73Arg
CA963765
NM_000110.4:c.218T>G