Canonical Allele Identifier:
CA337097229
Gene:
Linked Data
ClinVar Variation Id:
689982
ClinVar RCV Id:
RCV000850840
dbSNP Id:
rs9659239
MyVariant Identifiers:
chrMT:g.5773G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5773G>A , J01415.2:m.5773G>A | GRCh38 |