Your search for "lat2" returned 352 TaqMan® SNP Genotyping Assays
linker for activation of T-cells family member 2
This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]
AW125574, HSPC046, LAB, LAT2, NTAL, WBSCR15, WBSCR5, WSCR5
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