Linked Data
dbSNP Id:
rs2068713788
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9012T>C , J01415.2:m.9012T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.486T>C | ENSP00000354632.2:p.Ala162= |