Canonical Allele Identifier: CA645373342

Gene:

Linked Data

• ClinVar Variation Id: 430686
• ClinVar RCV Id: RCV000495253
• MyVariant Identifiers: chrMT:g.12114_14420del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12114_14420del , J01415.2:m.12114_14420del	GRCh38