Canonical Allele Identifier: CA128829

Gene:

Linked Data

• ClinVar Variation Id: 30002
• ClinVar RCV Id: RCV000022897
• dbSNP Id: rs387906732
• MyVariant Identifiers: chrMT:g.5816A>G (hg38)
• PubMed: PMID:17724295

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5816A>G , J01415.2:m.5816A>G	GRCh38