Canonical Allele Identifier: CA337096027

Gene:

Linked Data

• ClinVar Variation Id: 667050
• ClinVar RCV Id: RCV000825674
• dbSNP Id: rs879036775
• MyVariant Identifiers: chrMT:g.1303G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1303G>A , J01415.2:m.1303G>A	GRCh38