Canonical Allele Identifier: PA228079
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 88974
ClinVar RCV Id: RCV000086452 RCV000410600 RCV000500980 RCV000623094 RCV001787865 RCV001787336 RCV001787863 RCV001787864 RCV003915035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Asp949Val
CA228077
NM_000110.4:c.2846A>T