Canonical Allele Identifier: CA337099432

Gene:

Linked Data

• ClinVar Variation Id: 690187
• ClinVar RCV Id: RCV000851074
• dbSNP Id: rs386419957
• MyVariant Identifiers: chrMT:g.12285T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12285T>C , J01415.2:m.12285T>C	GRCh38