Canonical Allele Identifier: CA120560
Gene:

Linked Data

ClinVar Variation Id: 9589
ClinVar RCV Id: RCV000010206 RCV000010209 RCV000010211 RCV000010208 RCV000010210 RCV000022902 RCV000032997 RCV000022901 RCV000143997 RCV000224855 RCV000626561 RCV000495738 RCV000763623 RCV001794441 RCV002285005 RCV002287327 RCV002250458 RCV003325938 RCV003984803 RCV004554593
dbSNP Id: rs199474657
MyVariant Identifiers: chrMT:g.3243A>G (hg38)
PubMed: PMID:10356136 PMID:11085913 PMID:15372523 PMID:16950816 PMID:20301352 PMID:20301693 PMID:26822237
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3243A>G , J01415.2:m.3243A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'