Canonical Allele Identifier: CA645373337

Gene:

Linked Data

• ClinVar Variation Id: 430681
• ClinVar RCV Id: RCV000495437
• MyVariant Identifiers: chrMT:g.8587_12967del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8587_12967del , J01415.2:m.8587_12967del	GRCh38