Canonical Allele Identifier: PA2741809273
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 2587441
ClinVar RCV Id: RCV003344140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Ile636Thr
CA341375882
NM_000110.4:c.1907T>C