Canonical Allele Identifier: CA658653718

Gene:

Linked Data

• ClinVar Variation Id: 445831
• ClinVar RCV Id: RCV000513842
• dbSNP Id: rs1556422531
• MyVariant Identifiers: chrMT:g.1452T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1452T>C , J01415.2:m.1452T>C	GRCh38