Canonical Allele Identifier: CA250413

Gene:

Linked Data

• ClinVar Variation Id: 209212
• ClinVar RCV Id: RCV000191151
• MyVariant Identifiers: chrMT:g.5782_13922del (hg38)
• PubMed: PMID:24088041 ; PMID:26633545

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5782_13922del , J01415.2:m.5782_13922del	GRCh38