Canonical Allele Identifier:
CA337096467
Gene:
Linked Data
ClinVar Variation Id:
689857
ClinVar RCV Id:
RCV000850689
dbSNP Id:
rs879110136
MyVariant Identifiers:
chrMT:g.3248G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3248G>A , J01415.2:m.3248G>A | GRCh38 |