Linked Data
dbSNP Id:
rs2068749552
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15877C>T , J01415.2:m.15877C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361789.2:c.1131C>T | ENSP00000354554.2:p.Leu377= |