Linked Data
dbSNP Id:
rs2068689509
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4619T>C , J01415.2:m.4619T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361453.3:c.150T>C | ENSP00000355046.4:p.Pro50= |