Linked Data
dbSNP Id:
rs28358879
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.7624T>C , J01415.2:m.7624T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361739.1:c.39T>C | ENSP00000354876.1:p.Thr13= |