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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAA
(D282H)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type II
GPathogenic/Likely pathogenic
GAA
(M519T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GAA
(T711P)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type II
GLikely pathogenic
GAA
(R870*)
Single nucleotide variant
(nonsense)
Glycogen storage disease, type II
GPathogenic
GAA
(L901Q)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type II
GPathogenic
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