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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LYN
(G142V +1 more)
Single nucleotide variant
(missense variant)
Autoinflammatory disease, systemic, with vasculitis
GUncertain significance
LYN
(Y487H)
Single nucleotide variant
(missense variant)
Autoinflammatory disease, systemic, with vasculitis
GPathogenic
LYN
(Y487* +1 more)
Single nucleotide variant
(nonsense)
LYN kinase associated vasculopathy and liver fibrosis syndrome
+1 more
GPathogenic
LYN
(Y487F +1 more)
Single nucleotide variant
(missense variant)
Autoinflammatory disease, systemic, with vasculitis
+1 more
GPathogenic
LYN
(Q486* +1 more)
Single nucleotide variant
(nonsense)
LYN kinase associated vasculopathy and liver fibrosis syndrome
+1 more
GPathogenic
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