Linked Data
dbSNP Id:
rs1603222595
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9959T>C , J01415.2:m.9959T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000362079.2:c.753T>C | ENSP00000354982.2:p.Phe251= |