Canonical Allele Identifier: CA645373339

Gene:

Linked Data

• ClinVar Variation Id: 430683
• ClinVar RCV Id: RCV000495147
• MyVariant Identifiers: chrMT:g.8839_14895del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8839_14895del , J01415.2:m.8839_14895del	GRCh38