Canonical Allele Identifier:
CA337100571
Gene:
Linked Data
ClinVar Variation Id:
690226
ClinVar RCV Id:
RCV000851118
dbSNP Id:
rs41383248
MyVariant Identifiers:
chrMT:g.15907A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15907A>G , J01415.2:m.15907A>G | GRCh38 |