Linked Data
dbSNP Id:
rs1603218923
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3372T>C , J01415.2:m.3372T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361390.2:c.66T>C | ENSP00000354687.2:p.Leu22= |