Canonical Allele Identifier: CA120566

Gene:

Linked Data

• ClinVar Variation Id: 9596
• ClinVar RCV Id: RCV000850698 ; RCV004554596
• dbSNP Id: rs199474663
• MyVariant Identifiers: chrMT:g.3260A>G (hg38)
• ERepo: CA120566/MONDO:0044970/014
• PubMed: PMID:1677065 ; PMID:8132749

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3260A>G , J01415.2:m.3260A>G	GRCh38