Linked Data
dbSNP Id:
rs1556423700
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9620C>A , J01415.2:m.9620C>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362079.2:c.414C>A | ENSP00000354982.2:p.Leu138= |