| 11 | g.5225620G>T | CA124904 | HBB | c.422C>A (p.Ala141Asp)
c.*238C>A (n.*238C>A)
| ClinVar dbSNP |
| 11 | g.5225620G>A | CA125422 | HBB | c.422C>T (p.Ala141Val)
c.*238C>T (n.*238C>T)
| ClinVar dbSNP |
| 11 | g.5225620G= | CA1949564306 | HBB | c.422C= (p.Ala141=)
c.*238C= (n.*238C=)
| dbSNP |
