Canonical Allele Identifier: CA337097251

Gene:

Linked Data

• ClinVar Variation Id: 690005
• ClinVar RCV Id: RCV000850863
• dbSNP Id: rs56133209
• MyVariant Identifiers: chrMT:g.5821G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5821G>A , J01415.2:m.5821G>A	GRCh38