Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
19	g.7267825C>T	CA124247	INSR	c.172G>A (p.Gly58Arg) n.147G>A c.250G>A (p.Gly84Arg)	ClinVar dbSNP gnomAD v4
19	g.7267825C=	CA2320836555	INSR	c.172G= (p.Gly58=) n.147G= c.250G= (p.Gly84=)	dbSNP

Number of alleles fetched