Canonical Allele Identifier:
CA337099412
Gene:
Linked Data
ClinVar Variation Id:
690151
ClinVar RCV Id:
RCV000851034
dbSNP Id:
rs28505538
MyVariant Identifiers:
chrMT:g.12189T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12189T>C , J01415.2:m.12189T>C | GRCh38 |