Linked Data
dbSNP Id:
rs2124595097
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8925A>G , J01415.2:m.8925A>G | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.399A>G | ENSP00000354632.2:p.Thr133= |