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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AAAS
(P483L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
AAAS
(R478* +1 more)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder
+2 more
GPathogenic
AAAS
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic
AAAS
(E365fs +1 more)
Duplication
(frameshift variant)
AAAS-related condition
+2 more
GPathogenic
AAAS
(C180S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
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