Linked Data
ClinVar Variation Id:
805036
ClinVar RCV Id:
RCV000992348
dbSNP Id:
rs879089638
MyVariant Identifiers:
chrMT:g.7274C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.7274C>T , J01415.2:m.7274C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361624.2:c.1371C>T | ENSP00000354499.2:p.Gly457= |