Canonical Allele Identifier:
CA337100590
Gene:
Linked Data
ClinVar Variation Id:
690241
ClinVar RCV Id:
RCV000851135
dbSNP Id:
rs527236199
MyVariant Identifiers:
chrMT:g.15932T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15932T>C , J01415.2:m.15932T>C | GRCh38 |