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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126863137, MYH9
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC126863137, MYH9
(A958T)
Single nucleotide variant
(missense variant)
MYH9-related condition
+4 more
GConflicting classifications of pathogenicity
LOC126863137, MYH9
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GConflicting classifications of pathogenicity
LOC126863137, MYH9
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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