Linked Data
dbSNP Id:
rs1569484662
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.14584T>C , J01415.2:m.14584T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361681.2:c.90A>G | ENSP00000354665.2:p.Leu30= |