Linked Data
dbSNP Id:
rs1556424490
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.14774C>T , J01415.2:m.14774C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361789.2:c.28C>T | ENSP00000354554.2:p.Leu10= |