Canonical Allele Identifier: CA120586
Gene:

Linked Data

ClinVar Variation Id: 9623
ClinVar RCV Id: RCV000010249 RCV002247297
dbSNP Id: rs121434456
MyVariant Identifiers: chrMT:g.10438A>G (hg38)
PubMed: PMID:15286228
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10438A>G , J01415.2:m.10438A>G GRCh38
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