Canonical Allele Identifier: CA645373341

Gene:

Linked Data

• ClinVar Variation Id: 430685
• ClinVar RCV Id: RCV000494855
• MyVariant Identifiers: chrMT:g.11263_15374del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11263_15374del , J01415.2:m.11263_15374del	GRCh38