Canonical Allele Identifier: CA345913

Gene:

Linked Data

• ClinVar Variation Id: 155884
• ClinVar RCV Id: RCV000144003 ; RCV000850796
• dbSNP Id: rs1556423008
• MyVariant Identifiers: chrMT:g.5559A>G (hg38)
• PubMed: PMID:19349200 ; PMID:20301352

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5559A>G , J01415.2:m.5559A>G	GRCh38