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Mutations on the Protein: P16473 From Positions: 535 To 573

2
2
0
0




Swiss-Prot Disease: VAR_011538
p.ALA553THR
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 1 (CHNG1)


Swiss-Prot Disease: VAR_011539
p.ILE568THR
N/A
N/A
Hyperthyroidism, non-autoimmune (HTNA)






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