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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKN2A
(A109P +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+5 more
GUncertain significance
CDKN2A
(D84N +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+2 more
GConflicting classifications of pathogenicity
CDKN2A
(A68V +1 more)
Single nucleotide variant
(missense variant +2 more)
Familial melanoma
+3 more
GConflicting classifications of pathogenicity
CDKN2A
(I49T)
Single nucleotide variant
(missense variant +1 more)
CDKN2A-related condition
+8 more
GConflicting classifications of pathogenicity
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