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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT1
(T638S)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 1
GUncertain significance
KRT1
(L187P)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 1
GPathogenic
KRT1
(E478G)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 1
GPathogenic
KRT1
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic
KRT10, KRT10-AS1
(K439E)
Single nucleotide variant
(missense variant)
Epidermolytic hyperkeratosis 1
GPathogenic
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