Linked Data
dbSNP Id:
rs1569483877
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3387T>C , J01415.2:m.3387T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361390.2:c.81T>C | ENSP00000354687.2:p.Ile27= |