Canonical Allele Identifier: CA337097257

Gene:

Linked Data

• ClinVar Variation Id: 690008
• ClinVar RCV Id: RCV000850866
• dbSNP Id: rs879140945
• MyVariant Identifiers: chrMT:g.5824G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5824G>A , J01415.2:m.5824G>A	GRCh38