Human Genome Region UGT2B17
- Assembly:
- GRCh38.p14
- Location:
- chr4:68,306,359-69,010,457
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL000257.2 | NT_167250.2 | ALT | Unavailable | Unavailable | Unavailable | |