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Links from OMIM

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HMBS
(L81P +1 more)
Single nucleotide variant
(missense variant)
Encephalopathy, porphyria-related
GPathogenic
HMBS
(R201W +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
HMBS
(R167W +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
HMBS
(R173Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
HMBS
(R167Q +1 more)
Single nucleotide variant
(missense variant)
Acute intermittent porphyria
+1 more
GPathogenic/Likely pathogenic
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