Canonical Allele Identifier: PA108503
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Tyr449Asp
CA285513
NM_003060.4:c.1345T>G