Canonical Allele Identifier:
CA340924
Gene:
Linked Data
ClinVar Variation Id:
9574
ClinVar RCV Id:
RCV000010187
dbSNP Id:
rs118203886
MyVariant Identifiers:
chrMT:g.611G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.611G>A , J01415.2:m.611G>A | GRCh38 |