Canonical Allele Identifier:
CA120556
Gene:
MyVariant.info:
GRCh38
chrMT:g.8342G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8342G>A , J01415.2:m.8342G>A | GRCh38 |