Linked Data
dbSNP Id:
rs2068717801
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9641C>T , J01415.2:m.9641C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362079.2:c.435C>T | ENSP00000354982.2:p.Thr145= |