Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532711C>ACA122822RHOc.875C>A (p.Ala292Glu)
 ClinVar dbSNP
3g.129532711C>TCA354470722RHOc.875C>T (p.Ala292Val)
 ClinVar dbSNP

Number of alleles fetched