Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.53889901T>CCA9640291PRKCGc.413T>C (p.Val138Ala)
n.711T>C
n.715T>C
c.29T>C (p.Val10Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53889901T>ACA344640PRKCGc.413T>A (p.Val138Glu)
n.711T>A
n.715T>A
c.29T>A (p.Val10Glu)
 ClinVar dbSNP

Number of alleles fetched