Canonical Allele Identifier:
CA337097237
Gene:
Linked Data
ClinVar Variation Id:
689988
ClinVar RCV Id:
RCV000850846
dbSNP Id:
rs373493739
MyVariant Identifiers:
chrMT:g.5785T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5785T>C , J01415.2:m.5785T>C | GRCh38 |