Linked Data
dbSNP Id:
rs2068711841
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8766C>T , J01415.2:m.8766C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.240C>T | ENSP00000354632.2:p.Ala80= |