Canonical Allele Identifier: CA337097225

Gene:

Linked Data

• ClinVar Variation Id: 689979
• ClinVar RCV Id: RCV000850836
• dbSNP Id: rs2854138
• MyVariant Identifiers: chrMT:g.5711A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5711A>G , J01415.2:m.5711A>G	GRCh38