Canonical Allele Identifier: CA337097255

Gene:

Linked Data

• ClinVar Variation Id: 690007
• ClinVar RCV Id: RCV000850865
• dbSNP Id: rs878875817
• MyVariant Identifiers: chrMT:g.5823A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5823A>G , J01415.2:m.5823A>G	GRCh38