Canonical Allele Identifier:
CA337097828
Gene:
Linked Data
ClinVar Variation Id:
1526265
ClinVar RCV Id:
RCV002052285
dbSNP Id:
rs369704279
MyVariant Identifiers:
chrMT:g.8271_8279del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8281_8289del , J01415.2:m.8281_8289del | GRCh38 |