Canonical Allele Identifier:
CA337096875
Gene:
Linked Data
ClinVar Variation Id:
689915
ClinVar RCV Id:
RCV000850767
dbSNP Id:
rs377043134
MyVariant Identifiers:
chrMT:g.4452T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4452T>C , J01415.2:m.4452T>C | GRCh38 |