Canonical Allele Identifier: CA645373336

Gene:

Linked Data

• ClinVar Variation Id: 430680
• ClinVar RCV Id: RCV000495046 ; RCV000855712
• MyVariant Identifiers: chrMT:g.8483_13459del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8483_13459del , J01415.2:m.8483_13459del	GRCh38