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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH3
(D1574V)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
GUncertain significance
MYH3
(V923L)
Single nucleotide variant
(missense variant)
Freeman-Sheldon syndrome
+1 more
GUncertain significance
MYH3
(M823V)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
GUncertain significance
MYH3
(R672H)
Single nucleotide variant
(missense variant)
Freeman-Sheldon syndrome
+1 more
GPathogenic
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