Linked Data
dbSNP Id:
rs28358887
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8994G>T , J01415.2:m.8994G>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.468G>T | ENSP00000354632.2:p.Leu156= |