Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.52646750C>T	CA120291	KRT2	c.1459G>A (p.Glu487Lys)	ClinVar dbSNP gnomAD v4 COSMIC
12	g.52646750C>A	CA384929578	KRT2	c.1459G>T (p.Glu487Ter)	dbSNP gnomAD v2

Number of alleles fetched