Canonical Allele Identifier:
CA337100586
Gene:
Linked Data
ClinVar Variation Id:
690240
ClinVar RCV Id:
RCV000851134
dbSNP Id:
rs41441949
MyVariant Identifiers:
chrMT:g.15930G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15930G>A , J01415.2:m.15930G>A | GRCh38 |