beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein,BWR1A,BWSCR1A,efflux transporter-like protein,HET,imprinted multi-membrane-spanning polyspecific transporter-related protein 1,IMPT1,ITM,ORCTL2,organic cation transporter-like protein 2,p45 Beckwith-Wiedemann region 1A,p45-Beckwith-Wiedemann region 1 A,p45-BWR1A,SLC22A1L,solute carrier family 22 member 18,Solute carrier family 22 member 1-like,TSSC5,tumor-suppressing STF cDNA 5 protein,tumor-suppressing subchromosomal transferable fragment candidate gene 5 protein.
Homo sapiens solute carrier family 22 member 18 (SLC22A18), transcript variant 2, mRNA, Solute carrier family 22 member 18, solute carrier family 22 member 18 isoform b [Homo sapiens]
