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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM2, LOC130063529
(N3S)
Single nucleotide variant
(missense variant)
Centronuclear myopathy
GBenign
DNM2, LOC130063529
(R4C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DNM2, LOC130063529
(E7G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DNM2, LOC130063529
(K15R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130063529, DNM2
(N50S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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