Canonical Allele Identifier: CA337097243

Gene:

Linked Data

• ClinVar Variation Id: 689999
• ClinVar RCV Id: RCV000850857
• dbSNP Id: rs386828978
• MyVariant Identifiers: chrMT:g.5807A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5807A>G , J01415.2:m.5807A>G	GRCh38