Canonical Allele Identifier:
CA170533
Gene:
Linked Data
ClinVar Variation Id:
143904
ClinVar RCV Id:
RCV000133443
dbSNP Id:
rs527236199
MyVariant Identifiers:
chrMT:g.15932T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15932T>G , J01415.2:m.15932T>G | GRCh38 |