Canonical Allele Identifier: CA120568
Gene:

Linked Data

ClinVar Variation Id: 9598
ClinVar RCV Id: RCV000010221 RCV000850703 RCV002288480
dbSNP Id: rs199474666
MyVariant Identifiers: chrMT:g.3274A>G (hg38)
ERepo: CA120568/MONDO:0044970/014
PubMed: PMID:11723298
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3274A>G , J01415.2:m.3274A>G GRCh38
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