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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NALCN
(V566F +1 more)
Single nucleotide variant
(missense variant)
Arthrogryposis multiplex congenita
+1 more
GLikely pathogenic
NALCN
(F317C)
Single nucleotide variant
(missense variant)
Arthrogryposis multiplex congenita
+1 more
GLikely pathogenic
NALCN
(Y64C)
Single nucleotide variant
(missense variant)
Arthrogryposis multiplex congenita
+1 more
GLikely pathogenic
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