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Mutations on the Protein: NP_000360 From Positions: 382 To 420

2
0
0
2


OMIM Disease: 603372.0012
p.ASP410ASN
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1


OMIM Disease: 603372.0015
p.CYS390TRP
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1






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