Canonical Allele Identifier:
CA658653730
Gene:
Linked Data
ClinVar Variation Id:
441111
ClinVar RCV Id:
RCV000509522
dbSNP Id:
rs527236198
MyVariant Identifiers:
chrMT:g.15928G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15928G>T , J01415.2:m.15928G>T | GRCh38 |