Canonical Allele Identifier:
CA120559
Gene:
MyVariant.info:
GRCh38
chrMT:g.12297T>C
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12297T>C , J01415.2:m.12297T>C | GRCh38 |