Canonical Allele Identifier: CA337097240

Gene:

Linked Data

• ClinVar Variation Id: 689998
• ClinVar RCV Id: RCV000850856
• dbSNP Id: rs879211572
• MyVariant Identifiers: chrMT:g.5806T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5806T>C , J01415.2:m.5806T>C	GRCh38