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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP1A2
(G301R)
Single nucleotide variant
(missense variant)
Familial hemiplegic migraine
GPathogenic
ATP1A2
(D718N)
Single nucleotide variant
(missense variant)
Migraine, familial hemiplegic, 2
GLikely pathogenic
ATP1A2
(L764P)
Single nucleotide variant
(missense variant)
Migraine, familial hemiplegic, 2
GPathogenic
ATP1A2
(W887R)
Single nucleotide variant
(missense variant)
Migraine, familial hemiplegic, 2
GPathogenic
ATP1A2
(P979L)
Single nucleotide variant
(missense variant)
Familial hemiplegic migraine
+2 more
GPathogenic
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