Canonical Allele Identifier: PA2499228527
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 1209996
ClinVar RCV Id: RCV001579723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Met642Thr
CA341375841
NM_000110.4:c.1925T>C