Linked Data
dbSNP Id:
rs2124596974
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12022C>T , J01415.2:m.12022C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361381.2:c.1263C>T | ENSP00000354961.2:p.His421= |