Linked Data
dbSNP Id:
rs1556423594
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9031C>T , J01415.2:m.9031C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.505C>T | ENSP00000354632.2:p.Leu169= |