Canonical Allele Identifier:
CA337096873
Gene:
Linked Data
ClinVar Variation Id:
689912
ClinVar RCV Id:
RCV000850764
dbSNP Id:
rs878930498
MyVariant Identifiers:
chrMT:g.4435A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4435A>G , J01415.2:m.4435A>G | GRCh38 |