Hb Montgomery, an alpha globin chain variant due to CTG 48 CGG (Leu replaced by Arg) mutation on the alpha-2 globin gene, observed in a Caucasian baby girl.
- Cited forNUCLEOTIDE SEQUENCE
- TissueWhole blood
- CategoriesSequences
- SourceUniProtKB unreviewed (TrEMBL)
- SubmissionSubmitted to EMBL/GenBank/DDBJ databases ()
Cited in