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1 protein found in SwissVar (0 variants)

with gene/protein name P43699

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)
P43699 NKX21_HUMAN chorea, hereditary benign
P43699 NKX21_HUMAN choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction
P43699 NKX21_HUMAN thyroid cancer, non-medullary, 1