Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129531034G>ACA270023RHOc.520G>A (p.Gly174Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129531034G>CCA354498773RHOc.520G>C (p.Gly174Arg)
 ClinVar dbSNP
3g.129531034G=CA1401209653RHOc.520G= (p.Gly174=)
 dbSNP

Number of alleles fetched