Canonical Allele Identifier: PA645486237
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 298290
ClinVar RCV Id: RCV000385960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Ala513Gly
CA10610481
NM_000110.4:c.1538C>G