Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
17	g.50197027C>T	CA257875	COL1A1	c.787G>A (p.Gly263Arg) n.514G>A	ClinVar dbSNP
17	g.50197027C=	CA2263919563	COL1A1	c.787G= (p.Gly263=) n.514G=	dbSNP

Number of alleles fetched