Canonical Allele Identifier:
CA254837
Gene:
Linked Data
ClinVar Variation Id:
9583
ClinVar RCV Id:
RCV003162233
dbSNP Id:
rs118192101
MyVariant Identifiers:
chrMT:g.8313G>A (hg38)
ERepo:
CA254837/MONDO:0044970/014
PubMed:
PMID:9380435
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8313G>A , J01415.2:m.8313G>A | GRCh38 |