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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIN2A
(A1276G)
Single nucleotide variant
(missense variant +1 more)
Focal epilepsy
+5 more
GConflicting classifications of pathogenicity
GRIN2A
(N989S)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
+2 more
GConflicting classifications of pathogenicity
GRIN2A
(A716D)
Single nucleotide variant
(missense variant)
Landau-Kleffner syndrome
GUncertain significance
GRIN2A
(N380D)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GUncertain significance
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