Canonical Allele Identifier: PA228120
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 88975
ClinVar RCV Id: RCV000086474 RCV000410952 RCV001787866 RCV001787867 RCV001787868 RCV001787326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Ile560Ser
CA228118
NM_000110.4:c.1679T>G