Canonical Allele Identifier: CA259739
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 30001
dbSNP Id: rs200077222
MyVariant Identifiers: chrMT:g.5814T>C (hg38)

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5814T>C , J01415.2:m.5814T>C GRCh38