Human Genome Region NKRF
- Assembly:
- GRCh38.p14
- Location:
- chrX:119,549,000-119,689,565
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| MU273394.1 | Not yet assigned | FIX | Unavailable | Unavailable | Unavailable | |