Canonical Allele Identifier: PA645486326
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 298281
ClinVar RCV Id: RCV000299078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Ser878Gly
CA10610856
NM_000110.4:c.2632A>G