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
3g.129532711C=CA1401211971RHOc.875C= (p.Ala292=)
dbSNP

Number of alleles fetched