Linked Data
dbSNP Id:
rs1603222547
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9854T>C , J01415.2:m.9854T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362079.2:c.648T>C | ENSP00000354982.2:p.Thr216= |