Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.16129440G>ACA122981EPHA2c.2819C>T (p.Thr940Ile)
c.2657C>T (p.Thr886Ile)
 ClinVar dbSNP
1g.16129440G>CCA338615228EPHA2c.2819C>G (p.Thr940Ser)
c.2657C>G (p.Thr886Ser)
 dbSNP

Number of alleles fetched