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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIA2
(P336S +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with language impairment and behavioral abnormalities
GUncertain significance
GRIA2
(T353I +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with language impairment and behavioral abnormalities
GUncertain significance
GRIA2
(A760V +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with language impairment and behavioral abnormalities
GLikely pathogenic
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