Canonical Allele Identifier:
CA337096419
Gene:
Linked Data
ClinVar Variation Id:
441149
ClinVar RCV Id:
RCV000509285
dbSNP Id:
rs3928306
MyVariant Identifiers:
chrMT:g.3010G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3010G>A , J01415.2:m.3010G>A | GRCh38 |