Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129529002G>ACA122823RHOc.269G>A (p.Gly90Asp)
ClinVar dbSNP
3g.129529002G>TCA354496638RHOc.269G>T (p.Gly90Val)
dbSNP gnomAD v4
3g.129529002G=CA1401205916RHOc.269G= (p.Gly90=)
dbSNP

Number of alleles fetched