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1 protein found in SwissVar (0 variants)

with gene/protein name Q96N87

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
Q96N87 S6A18_HUMAN disease phentotype in some individuals with iminoglycinuria or hyperglycinuria, that carry variants in slc36a2, slc6a19 or slc6a20