Linked Data
dbSNP Id:
rs1603222998
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.10877C>T , J01415.2:m.10877C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361381.2:c.118C>T | ENSP00000354961.2:p.Leu40= |