Canonical Allele Identifier: CA645373331

Gene:

Linked Data

• ClinVar Variation Id: 430674
• ClinVar RCV Id: RCV000495067
• MyVariant Identifiers: chrMT:g.6003_11220del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.6005_11222del , J01415.2:m.6005_11222del	GRCh38