Canonical Allele Identifier:
CA337097834
Gene:
Linked Data
ClinVar Variation Id:
690066
ClinVar RCV Id:
RCV000850940
dbSNP Id:
rs879081228
MyVariant Identifiers:
chrMT:g.8308A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8308A>G , J01415.2:m.8308A>G | GRCh38 |