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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NINL
(E782*)
Single nucleotide variant
(nonsense +1 more)
Autism spectrum disorder
GUncertain significance
NINL
(Q696*)
Single nucleotide variant
(nonsense)
Autism spectrum disorder
GUncertain significance