Canonical Allele Identifier: PA2580103380
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 1804875
ClinVar RCV Id: RCV002470172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Pro237Leu
CA963579
NM_000110.4:c.710C>T