Canonical Allele Identifier: CA645373335

Gene:

Linked Data

• ClinVar Variation Id: 430678
• ClinVar RCV Id: RCV000495493
• MyVariant Identifiers: chrMT:g.8290_13040del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8290_13040del , J01415.2:m.8290_13040del	GRCh38