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Mutations on the Protein: Q06710 From Positions: 45 To 68

6
2
0
4





Swiss-Prot Disease: VAR_012771
p.CYS57TYR
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 2 (CHNG2)


Swiss-Prot Disease: VAR_012772
p.LEU62ARG
N/A
N/A
Hypothyroidism, congenital, non-goitrous, 2 (CHNG2)


OMIM Disease: 167415.0005
p.CYS57TYR
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0004
p.LEU62ARG
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0006
p.SER54GLY
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0008
p.SER48PHE
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2






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