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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCTN1
(V558M +6 more)
Single nucleotide variant
(missense variant +1 more)
Amyotrophic lateral sclerosis type 1
GUncertain significance
DCTN1
(P157L +6 more)
Single nucleotide variant
(missense variant +1 more)
Perry syndrome
+4 more
GUncertain significance