Canonical Allele Identifier:
CA337100611
Gene:
Linked Data
ClinVar Variation Id:
690259
ClinVar RCV Id:
RCV000851155
dbSNP Id:
rs199993959
MyVariant Identifiers:
chrMT:g.15951A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15951A>G , J01415.2:m.15951A>G | GRCh38 |