Canonical Allele Identifier:
CA337100627
Gene:
Linked Data
ClinVar Variation Id:
1684921
ClinVar RCV Id:
RCV002248013
dbSNP Id:
rs55934780
MyVariant Identifiers:
chrMT:g.16023G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.16023G>A , J01415.2:m.16023G>A | GRCh38 |