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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806427, TTN
(D12499N +5 more)
Single nucleotide variant
(missense variant)
not specified
+7 more
GUncertain significance
LOC126806427, TTN
(S15043N +5 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+7 more
GUncertain significance
LOC126806427, TTN
(N12433H +5 more)
Single nucleotide variant
(missense variant)
not specified
+7 more
GUncertain significance
LOC126806427, TTN
Single nucleotide variant
(synonymous variant)
not specified
+7 more
GConflicting classifications of pathogenicity
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