Canonical Allele Identifier: PA108153
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 6427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Arg399Trp
CA312953
NM_003060.4:c.1195C>T