Linked Data
dbSNP Id:
rs1569484519
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12468T>C , J01415.2:m.12468T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361567.2:c.132T>C | ENSP00000354813.2:p.Phe44= |