Canonical Allele Identifier:
CA120569
Gene:
MyVariant.info:
GRCh38
chrMT:g.4317A>G
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4317A>G , J01415.2:m.4317A>G | GRCh38 |