Canonical Allele Identifier:
CA337100791
Gene:
Linked Data
ClinVar Variation Id:
1525975
ClinVar RCV Id:
RCV002037091
dbSNP Id:
rs2853514
MyVariant Identifiers:
chrMT:g.16230A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.16230A>G , J01415.2:m.16230A>G | GRCh38 |