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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LIN52
(A36V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LIN52
(P51R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LIN52
(R59H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LIN52
(D61N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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