Canonical Allele Identifier:
CA337095922
Gene:
Linked Data
ClinVar Variation Id:
805059
ClinVar RCV Id:
RCV000992381
dbSNP Id:
rs56489998
MyVariant Identifiers:
chrMT:g.663A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.663A>G , J01415.2:m.663A>G | GRCh38 |