Canonical Allele Identifier: CA645373333

Gene:

Linked Data

• ClinVar Variation Id: 430676
• ClinVar RCV Id: RCV000495692
• MyVariant Identifiers: chrMT:g.7129_13991del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7129_13991del , J01415.2:m.7129_13991del	GRCh38