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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130056876, RHOV
(P11S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LOC130056876, RHOV
(T18P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(S25R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(A26T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(G40S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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