Canonical Allele Identifier:
CA170531
Gene:
Linked Data
ClinVar Variation Id:
143901
ClinVar RCV Id:
RCV000133440
dbSNP Id:
rs527236196
MyVariant Identifiers:
chrMT:g.15890C>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15890C>A , J01415.2:m.15890C>A | GRCh38 |