Your search for "slc6a19" returned 170 TaqMan® SNP Genotyping Assays
solute carrier family 6 member 19
This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]
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