Linked Data
dbSNP Id:
rs1603219902
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5327C>T , J01415.2:m.5327C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361453.3:c.858C>T | ENSP00000355046.4:p.Thr286= |