Linked Data
dbSNP Id:
rs1603221367
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8266A>G , J01415.2:m.8266A>G | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361739.1:c.681A>G | ENSP00000354876.1:p.Leu227= |