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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GH-LCR, SCN4A
(A1801T)
Single nucleotide variant
(missense variant)
Paramyotonia congenita of Von Eulenburg
+5 more
GConflicting classifications of pathogenicity
GH-LCR, SCN4A
(R1448H)
Single nucleotide variant
(missense variant)
Delayed gross motor development
+3 more
GPathogenic
SCN4A
(E452K)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
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