Canonical Allele Identifier: CA645373334

Gene:

Linked Data

• ClinVar Variation Id: 430677
• ClinVar RCV Id: RCV000495092
• MyVariant Identifiers: chrMT:g.7730_11255del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7731_11256del , J01415.2:m.7731_11256del	GRCh38