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Mutations on the Protein: NP_000360 From Positions: 535 To 573

2
0
0
2




OMIM Disease: 603372.0016
p.ALA553THR
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1


OMIM Disease: 603372.0010
p.TRP546TER
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1






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