Linked Data
dbSNP Id:
rs2124596530
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.11089C>T , J01415.2:m.11089C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361381.2:c.330C>T | ENSP00000354961.2:p.Phe110= |