Canonical Allele Identifier:
CA337095814
Gene:
dbSNP:
MyVariant.info:
GRCh38
chrMT:g.295C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.295C>T , J01415.2:m.295C>T | GRCh38 |