Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.177380T>GCA125955HBA1c.398T>G (p.Val133Gly)
c.302T>G (p.Val101Gly)
n.534T>G
 ClinVar dbSNP
16g.177380T=CA2200883303HBA1c.398T= (p.Val133=)
c.302T= (p.Val101=)
n.534T=
 dbSNP

Number of alleles fetched