Canonical Allele Identifier: CA259740
Gene:

Linked Data

ClinVar Variation Id: 30004
ClinVar RCV Id: RCV000022899 RCV000851039 RCV003319172
dbSNP Id: rs387906733
MyVariant Identifiers: chrMT:g.12201T>C (hg38)
PubMed: PMID:21931169
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12201T>C , J01415.2:m.12201T>C GRCh38
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