Linked Data
dbSNP Id:
rs1556424331
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.13812T>C , J01415.2:m.13812T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361567.2:c.1476T>C | ENSP00000354813.2:p.Ala492= |