Canonical Allele Identifier: CA120550

Gene:

Linked Data

• ClinVar Variation Id: 9572
• ClinVar RCV Id: RCV000010185 ; RCV000851158
• dbSNP Id: rs199474701
• MyVariant Identifiers: chrMT:g.15967G>A (hg38)
• PubMed: PMID:19273760 ; PMID:20301693

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15967G>A , J01415.2:m.15967G>A	GRCh38