Canonical Allele Identifier:
CA337100619
Gene:
Linked Data
ClinVar Variation Id:
690262
ClinVar RCV Id:
RCV000851160
dbSNP Id:
rs375213730
MyVariant Identifiers:
chrMT:g.15970T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15970T>C , J01415.2:m.15970T>C | GRCh38 |