Canonical Allele Identifier: CA645373340

Gene:

Linked Data

• ClinVar Variation Id: 430684
• ClinVar RCV Id: RCV000495541
• MyVariant Identifiers: chrMT:g.10106_15067del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10106_15067del , J01415.2:m.10106_15067del	GRCh38