Linked Data
dbSNP Id:
rs1603221544
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8506T>C , J01415.2:m.8506T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361851.1:c.141T>C | ENSP00000355265.1:p.Tyr47= |