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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NKX2-6
(E197K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NKX2-6
(P160R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NKX2-6
(A146V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NKX2-6
(R51Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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