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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SH3TC2
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign
SH3TC2
(V1158I)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease type 4
+5 more
GBenign
SH3TC2
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease type 4
+5 more
GBenign
SH3TC2
(A468S)
Single nucleotide variant
(missense variant)
not provided
+5 more
GBenign
SH3TC2
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease type 4
+5 more
GBenign
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