Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130872883T>CCA122587ABL1c.988T>C (p.Phe330Leu)
c.931T>C (p.Phe311Leu)
 ClinVar dbSNP COSMIC
9g.130872883T=CA1881475977ABL1c.988T= (p.Phe330=)
c.931T= (p.Phe311=)
 dbSNP

Number of alleles fetched