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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP6V1A
(G83D)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy, infantile or early childhood, 3
GUncertain significance
ATP6V1A
(V199A)
Single nucleotide variant
(missense variant)
ATP6V1A-related condition
+2 more
GUncertain significance
ATP6V1A
(P446L)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy, infantile or early childhood, 3
+1 more
GUncertain significance
ATP6V1A
(V511A)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy, infantile or early childhood, 3
GUncertain significance
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