Canonical Allele Identifier: CA337097653

Gene:

Linked Data

• ClinVar Variation Id: 690059
• ClinVar RCV Id: RCV000850932
• dbSNP Id: rs201582552
• MyVariant Identifiers: chrMT:g.7581T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7581T>C , J01415.2:m.7581T>C	GRCh38