Canonical Allele Identifier:
CA337100561
Gene:
Linked Data
ClinVar Variation Id:
690221
ClinVar RCV Id:
RCV000851113
dbSNP Id:
rs878927456
MyVariant Identifiers:
chrMT:g.15900T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15900T>C , J01415.2:m.15900T>C | GRCh38 |