Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862977A>TCA16602552ABL1c.821A>T (p.Glu274Val)
c.764A>T (p.Glu255Val)
ClinVar dbSNP COSMIC
9g.130862977A=CA1881463524ABL1c.821A= (p.Glu274=)
c.764A= (p.Glu255=)
dbSNP

Number of alleles fetched