Canonical Allele Identifier: CA645373332

Gene:

Linked Data

• ClinVar Variation Id: 430675
• ClinVar RCV Id: RCV000495334
• MyVariant Identifiers: chrMT:g.6469_15587del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.6470_15588del , J01415.2:m.6470_15588del	GRCh38