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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMC2
(R165C)
Single nucleotide variant
(missense variant)
Amelogenesis imperfecta type 1
+4 more
GConflicting classifications of pathogenicity
COL7A1
(M1262T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
COL7A1
(R1202H)
Single nucleotide variant
(missense variant)
Amelogenesis imperfecta type 1
+2 more
GConflicting classifications of pathogenicity
COL7A1
Single nucleotide variant
(intron variant)
Amelogenesis imperfecta type 1
GUncertain significance
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