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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT6B
(E472K)
Single nucleotide variant
(missense variant)
Pachyonychia congenita 4
+1 more
GPathogenic
KRT6B
(E461K)
Single nucleotide variant
(missense variant)
Pachyonychia congenita 4
+1 more
GPathogenic/Likely pathogenic
KRT6B
(N172del)
Microsatellite
(inframe_deletion)
Pachyonychia congenita 4
+1 more
GPathogenic
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