Canonical Allele Identifier: PA2741809283
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 2587443
ClinVar RCV Id: RCV003344142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Thr779Ala
CA341374597
NM_000110.4:c.2335A>G