Canonical Allele Identifier: PA102071
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 298300
ClinVar RCV Id: RCV000362597 RCV000786703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Arg235Trp
CA963582
NM_000110.4:c.703C>T