Canonical Allele Identifier:
CA337095804
Gene:
Linked Data
ClinVar Variation Id:
441147
ClinVar RCV Id:
RCV000509228
dbSNP Id:
rs2853515
MyVariant Identifiers:
chrMT:g.263A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.263A>G , J01415.2:m.263A>G | GRCh38 |