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Links from Gene

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862621, PRKCA
Single nucleotide variant
(synonymous variant)
PRKCA-related disorder
GLikely benign
LOC126862621, PRKCA
(I162V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRKCA
Copy number loss
not provided
GUncertain significance
PRKCA
Copy number loss
not provided
GUncertain significance
LOC126862621, PRKCA
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
PRKCA
Copy number loss
not provided
GUncertain significance
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