Canonical Allele Identifier:
CA337095880
Gene:
MyVariant.info:
GRCh38
chrMT:g.489T>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.489T>C , J01415.2:m.489T>C | GRCh38 |