Canonical Allele Identifier:
CA414823975
Gene:
Linked Data
ClinVar Variation Id:
690236
ClinVar RCV Id:
RCV000851128
dbSNP Id:
rs193303001
MyVariant Identifiers:
chrMT:g.15924A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15924A>G , J01415.2:m.15924A>G | GRCh38 |