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Mutations on the Protein: NP_000360 From Positions: 306 To 344

2
0
0
2


OMIM Disease: 603372.0027
p.ARG310CYS
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1


OMIM Disease: 603372.0011
p.GLN324TER
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1






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