Canonical Allele Identifier: CA645373338

Gene:

Linked Data

• ClinVar Variation Id: 430682
• ClinVar RCV Id: RCV000494750
• MyVariant Identifiers: chrMT:g.8815_13722del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8815_13722del , J01415.2:m.8815_13722del	GRCh38