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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2A
(P1359L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
GRIN2A
(S1312R)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
GRIN2A
(L1052F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRIN2A
(G928V)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
+1 more
GUncertain significance
GRIN2A
(N35T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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