Linked Data
dbSNP Id:
rs1603225050
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15055T>C , J01415.2:m.15055T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361789.2:c.309T>C | ENSP00000354554.2:p.Tyr103= |