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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GYS1
(P479L +1 more)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
GUncertain significance
GYS1
(T371A +1 more)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
GUncertain significance
GYS1
(D351N +1 more)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
+2 more
GUncertain significance
GYS1
(T395M +1 more)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
GUncertain significance
GYS1
(R105H)
Single nucleotide variant
(missense variant +2 more)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
GUncertain significance
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