Linked Data
dbSNP Id:
rs2068712256
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8823T>C , J01415.2:m.8823T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.297T>C | ENSP00000354632.2:p.Ser99= |