Linked Data
dbSNP Id:
rs2068744257
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.14965A>G , J01415.2:m.14965A>G | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361789.2:c.219A>G | ENSP00000354554.2:p.Val73= |