Linked Data
dbSNP Id:
rs1556422817
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4131A>C , J01415.2:m.4131A>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361390.2:c.825A>C | ENSP00000354687.2:p.Thr275= |