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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HADHB
(S154* +2 more)
Single nucleotide variant
(nonsense)
Mitochondrial trifunctional protein deficiency 2
GLikely pathogenic
HADHB
(R195Q +2 more)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency 2
+2 more
GUncertain significance
HADHB
(R229* +2 more)
Single nucleotide variant
(nonsense)
Mitochondrial trifunctional protein deficiency
+1 more
GPathogenic
HADHB
(N396D +2 more)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency 2
GUncertain significance
HADHB
(M445L +2 more)
Single nucleotide variant
(missense variant)
Mitochondrial trifunctional protein deficiency 2
GUncertain significance
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