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Mutations on the Protein: NP_000360 From Positions: 458 To 497

2
0
0
2




OMIM Disease: 603372.0030
p.LEU467PRO
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1


OMIM Disease: 603372.0026
p.THR477ILE
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1






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