Canonical Allele Identifier:
CA337099410
Gene:
Linked Data
ClinVar Variation Id:
690150
ClinVar RCV Id:
RCV000851033
dbSNP Id:
rs879128211
MyVariant Identifiers:
chrMT:g.12188T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12188T>C , J01415.2:m.12188T>C | GRCh38 |