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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASR
(R172S)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia 1
GUncertain significance
CASR
(W530*)
Single nucleotide variant
(nonsense)
Hypocalcemia
GPathogenic
CASR
(C575R +1 more)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia 1
GUncertain significance
CASR
(T780N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASR
(H879Q +1 more)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia 1
GUncertain significance
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