Human Genome Region TGOLN2
- Assembly:
- GRCh38.p14
- Location:
- chr2:85,073,815-85,358,733
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| MU273340.1 | Not yet assigned | NOVEL | Unavailable | Unavailable | Unavailable | |