Canonical Allele Identifier: CA337095948

Gene:

Linked Data

• ClinVar Variation Id: 805060
• ClinVar RCV Id: RCV000992382
• dbSNP Id: rs878985110
• MyVariant Identifiers: chrMT:g.813A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.813A>G , J01415.2:m.813A>G	GRCh38