Canonical Allele Identifier:
CA130991
Gene:
Linked Data
ClinVar Variation Id:
42204
ClinVar RCV Id:
RCV000035028
dbSNP Id:
rs2000974
MyVariant Identifiers:
chrMT:g.1048C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.1048C>T , J01415.2:m.1048C>T | GRCh38 |