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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOG
(E127*)
Single nucleotide variant
(nonsense)
Brachydactyly type B2
+1 more
GPathogenic/Likely pathogenic
NOG
(R204Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NOG
(P35A)
Single nucleotide variant
(missense variant)
Brachydactyly type B2
GPathogenic
NOG
(P35S)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
NOG
(R167G)
Single nucleotide variant
(missense variant)
Brachydactyly type B2
GPathogenic
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