Linked Data
dbSNP Id:
rs2068739989
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.14185A>C , J01415.2:m.14185A>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361681.2:c.489T>G | ENSP00000354665.2:p.Gly163= |