Canonical Allele Identifier:
CA337100576
Gene:
Linked Data
ClinVar Variation Id:
690227
ClinVar RCV Id:
RCV000851119
dbSNP Id:
rs386829266
MyVariant Identifiers:
chrMT:g.15908T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15908T>C , J01415.2:m.15908T>C | GRCh38 |