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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806426, TTN
+1 more
(R16339W +5 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
LOC126806426, TTN
+1 more
(V13714I +5 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GConflicting classifications of pathogenicity
LOC126806426, TTN
+1 more
(R14587H +5 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
LOC126806426, TTN
+1 more
(K13655Q +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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