Canonical Allele Identifier: CA337099427

Gene:

Linked Data

• ClinVar Variation Id: 690174
• ClinVar RCV Id: RCV000851061
• dbSNP Id: rs202114991
• MyVariant Identifiers: chrMT:g.12248A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12248A>G , J01415.2:m.12248A>G	GRCh38