Canonical Allele Identifier: CA128831

Gene:

Linked Data

• ClinVar Variation Id: 30005
• ClinVar RCV Id: RCV000022903 ; RCV000850632
• dbSNP Id: rs387906734
• MyVariant Identifiers: chrMT:g.586G>A (hg38)
• PubMed: PMID:21060018

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.586G>A , J01415.2:m.586G>A	GRCh38