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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HADHB
(R61H +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
HADHB
(N92S +2 more)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency
+1 more
GConflicting classifications of pathogenicity
HADHB
(V143I +2 more)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency
+1 more
GUncertain significance
HADHB
Single nucleotide variant
(splice acceptor variant)
Mitochondrial trifunctional protein deficiency 2
+1 more
GPathogenic/Likely pathogenic
HADHB
(R247H +2 more)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency
+1 more
GPathogenic/Likely pathogenic
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