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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALK
(I1461V +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
ALK
(E1435del +1 more)
Microsatellite
(inframe_deletion)
Neuroblastoma Susceptibility
+3 more
GBenign/Likely benign
ALK
(A1396T +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
ALK
Single nucleotide variant
(intron variant)
Neuroblastoma, susceptibility to, 3
+2 more
GBenign
ALK
Duplication
(intron variant)
Familial isolated pituitary adenoma
+4 more
GBenign/Likely benign
ALK
Single nucleotide variant
(synonymous variant)
ALK-related condition
+3 more
GConflicting classifications of pathogenicity
ALK
Single nucleotide variant
(intron variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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