Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
9	g.101371179T>C	CA118444	BAAT	c.226A>G (p.Met76Val)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9	g.101371179T>G	CA374256640	BAAT	c.226A>C (p.Met76Leu)	dbSNP
9	g.101371179T=	CA1868214036	BAAT	c.226A= (p.Met76=)	dbSNP

Number of alleles fetched