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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1A
(S1799L +3 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
CACNA1A
(I613M +1 more)
Single nucleotide variant
(missense variant)
Migraine, familial hemiplegic, 1
+3 more
GLikely pathogenic