Canonical Allele Identifier:
CA337100584
Gene:
Linked Data
ClinVar Variation Id:
690239
ClinVar RCV Id:
RCV000851133
dbSNP Id:
rs878866272
MyVariant Identifiers:
chrMT:g.15929A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15929A>G , J01415.2:m.15929A>G | GRCh38 |