Canonical Allele Identifier: CA120539
Gene:

Linked Data

ClinVar Variation Id: 9553
ClinVar RCV Id: RCV000010162 RCV000850873
dbSNP Id: rs118203894
MyVariant Identifiers: chrMT:g.5843A>G (hg38)
PubMed: PMID:14598342
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5843A>G , J01415.2:m.5843A>G GRCh38
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