Canonical Allele Identifier: CA113778

Gene:

Linked Data

• ClinVar Variation Id: 143864
• ClinVar RCV Id: RCV000133403
• dbSNP Id: rs527236161
• MyVariant Identifiers: chrMT:g.14743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14743A>G , J01415.2:m.14743A>G	GRCh38