Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.188989424G>T	CA007226	COL3A1	c.665G>T (p.Gly222Val)	ClinVar dbSNP
2	g.188989424G>A	CA007217	COL3A1	c.665G>A (p.Gly222Asp)	ClinVar dbSNP gnomAD v4

Number of alleles fetched