Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862955C>GCA16602546ABL1c.799C>G (p.Leu267Val)
c.742C>G (p.Leu248Val)
ClinVar dbSNP COSMIC
9g.130862955C>ACA375263219ABL1c.799C>A (p.Leu267Met)
c.742C>A (p.Leu248Met)
dbSNP

Number of alleles fetched