Canonical Allele Identifier: CA658799933

Gene:

Linked Data

• ClinVar Variation Id: 505294
• ClinVar RCV Id: RCV000610516
• dbSNP Id: rs1556422516
• MyVariant Identifiers: chrMT:g.1284T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1284T>C , J01415.2:m.1284T>C	GRCh38