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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO38
(D443G)
Single nucleotide variant
(missense variant)
Neuronopathy, distal hereditary motor, type 2D
GLikely benign
FBXO38
(D573Y)
Single nucleotide variant
(missense variant)
Neuronopathy, distal hereditary motor, type 2D
GUncertain significance
FBXO38
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
FBXO38
(P837A +2 more)
Single nucleotide variant
(missense variant)
Neuronopathy, distal hereditary motor, type 2D
GUncertain significance
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