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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A1
(A38fs)
Deletion
(frameshift variant +1 more)
Myasthenic syndrome, congenital, 23, presynaptic
GLikely pathogenic
SLC25A1
(C41R +1 more)
Single nucleotide variant
(missense variant +2 more)
Myasthenic syndrome, congenital, 23, presynaptic
GLikely pathogenic
SLC25A1
(D69Y +1 more)
Single nucleotide variant
(missense variant +2 more)
Myasthenic syndrome, congenital, 23, presynaptic
GUncertain significance
SLC25A1
(R247Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Myasthenic syndrome, congenital, 23, presynaptic
GPathogenic
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