Canonical Allele Identifier: PA1139699299
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 976091
ClinVar RCV Id: RCV001253275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Pro786His
CA341374555
NM_000110.4:c.2357C>A