Canonical Allele Identifier:
CA16040645
Gene:
MyVariant.info:
GRCh38
chrMT:g.3275C>T
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3275C>T , J01415.2:m.3275C>T | GRCh38 |