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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MVP-DT, PRRT2
(R217fs)
Duplication
(frameshift variant)
Seizure
+13 more
GPathogenic/Likely pathogenic
MVP-DT, PRRT2
Single nucleotide variant
(3 prime UTR variant +1 more)
Episodic kinesigenic dyskinesia
+4 more
GPathogenic/Likely pathogenic
MVP-DT, PRRT2
(G324V)
Single nucleotide variant
(missense variant +1 more)
Episodic kinesigenic dyskinesia and familial infantile convulsions with paroxysmal choreoathetosis
+1 more
GLikely pathogenic
MVP-DT, PRRT2
(E339D)
Single nucleotide variant
(missense variant +2 more)
Episodic kinesigenic dyskinesia 1
GUncertain significance
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