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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERBB4
(R1275W +1 more)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
ERBB4
(R927Q)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 19
+1 more
GPathogenic