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Mutations on the Protein: NP_054698 From Positions: 29 To 43

2
0
0
2





OMIM Disease: 167415.0003
p.ARG31HIS
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0007
p.GLN40PRO
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2






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