Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
13	g.27924439G>A	CA119970	PDX1	c.590G>A (p.Arg197His)	ClinVar dbSNP
13	g.27924439G=	CA2080721271	PDX1	c.590G= (p.Arg197=)	dbSNP
13	g.27924439G>T	CA387645942	PDX1	c.590G>T (p.Arg197Leu)	dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched