Canonical Allele Identifier:
CA337095860
Gene:
MyVariant.info:
GRCh38
chrMT:g.456C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.456C>T , J01415.2:m.456C>T | GRCh38 |