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Mutations on the Protein: P16473 From Positions: 153 To 191

3
3
0
0


Swiss-Prot Disease: VAR_011522
p.ILE167ASN
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 1 (CHNG1)


Swiss-Prot Disease: VAR_003566
p.LYS183ARG
N/A
N/A
Familial gestational hyperthyroidism (HTFG)


Swiss-Prot Disease: VAR_011521
p.PRO162ALA
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 1 (CHNG1)






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