Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129531005C>ACA256689RHOc.491C>A (p.Ala164Glu)
 ClinVar dbSNP
3g.129531005C>TCA16616904RHOc.491C>T (p.Ala164Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched