Canonical Allele Identifier:
CA337097263
Gene:
Linked Data
ClinVar Variation Id:
690009
ClinVar RCV Id:
RCV000850867
dbSNP Id:
rs386828979
MyVariant Identifiers:
chrMT:g.5836A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5836A>G , J01415.2:m.5836A>G | GRCh38 |