Canonical Allele Identifier:
CA337100902
Gene:
dbSNP:
MyVariant.info:
GRCh38
chrMT:g.16311T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.16311T>C , J01415.2:m.16311T>C | GRCh38 |