Canonical Allele Identifier:
CA337096131
Gene:
MyVariant.info:
GRCh38
chrMT:g.1719G>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.1719G>A , J01415.2:m.1719G>A | GRCh38 |