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1 protein found in SwissVar (0 variants)

with gene/protein name P51795

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)
P51795 CLCN5_HUMAN hypophosphatemic rickets, x-linked recessive
P51795 CLCN5_HUMAN nephrolithiasis 2
P51795 CLCN5_HUMAN nephrolithiasis 1
P51795 CLCN5_HUMAN low molecular weight proteinuria with hypercalciuria and nephrocalcinosis