Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129533710C>TCA256663RHOc.1039C>T (p.Pro347Ser)
ClinVar dbSNP
3g.129533710C>ACA354471278RHOc.1039C>A (p.Pro347Thr)
ClinVar dbSNP
3g.129533710C>GCA354471279RHOc.1039C>G (p.Pro347Ala)
ClinVar dbSNP
3g.129533710C=CA1401213449RHOc.1039C= (p.Pro347=)
dbSNP

Number of alleles fetched