Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130872961G>ACA16609341ABL1c.1066G>A (p.Ala356Thr)
c.1009G>A (p.Ala337Thr)
ClinVar dbSNP
9g.130872961G=CA1881476100ABL1c.1066G= (p.Ala356=)
c.1009G= (p.Ala337=)
dbSNP

Number of alleles fetched