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Mutations on the Protein: Q06710 From Positions: 23 To 45

4
2
0
2





Swiss-Prot Disease: VAR_012769
p.ARG31HIS
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 2 (CHNG2)


Swiss-Prot Disease: VAR_012770
p.GLN40PRO
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 2 (CHNG2)


OMIM Disease: 167415.0003
p.ARG31HIS
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0007
p.GLN40PRO
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2






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