Canonical Allele Identifier:
CA645373338
Gene:
MyVariant.info:
GRCh38
chrMT:g.8815_13722del
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8815_13722del , J01415.2:m.8815_13722del | GRCh38 |