Canonical Allele Identifier: PA200994
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 100092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Ile543Val
CA200992
NM_000110.4:c.1627A>G