Linked Data
dbSNP Id:
rs1603220187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5927C>T , J01415.2:m.5927C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361624.2:c.24C>T | ENSP00000354499.2:p.Phe8= |