Linked Data
dbSNP Id:
rs1603221043
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.7627C>T , J01415.2:m.7627C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361739.1:c.42C>T | ENSP00000354876.1:p.Ser14= |