Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.129529049G>T	CA256669	RHO	c.316G>T (p.Gly106Trp)	ClinVar dbSNP
3	g.129529049G>C	CA354496864	RHO	c.316G>C (p.Gly106Arg)	ClinVar dbSNP
3	g.129529049G>A	CA256683	RHO	c.316G>A (p.Gly106Arg)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched