Canonical Allele Identifier: PA228073
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 100069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Pro1023Thr
CA228071
NM_000110.4:c.3067C>A