Canonical Allele Identifier:
CA254840
Gene:
Linked Data
ClinVar Variation Id:
9599
ClinVar RCV Id:
RCV000010222
dbSNP Id:
rs199474667
MyVariant Identifiers:
chrMT:g.3249G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3249G>A , J01415.2:m.3249G>A | GRCh38 |