Linked Data
dbSNP Id:
rs2068747839
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15574C>T , J01415.2:m.15574C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361789.2:c.828C>T | ENSP00000354554.2:p.Phe276= |