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Mutations on the Protein: NP_000360 From Positions: 497 To 535

3
0
0
3




OMIM Disease: 603372.0014
p.PHE525LEU
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1


OMIM Disease: 603372.0021
p.SER505ASN
N/A
N/A
HYPERTHYROIDISM, NONAUTOIMMUNE


OMIM Disease: 603372.0019
p.VAL509ALA
N/A
N/A
HYPERTHYROIDISM, NONAUTOIMMUNE






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