Canonical Allele Identifier: CA120545
Gene:

Linked Data

ClinVar Variation Id: 9561
ClinVar RCV Id: RCV000010173 RCV002247285
dbSNP Id: rs118203889
MyVariant Identifiers: chrMT:g.12207G>A (hg38)
PubMed: PMID:16950817
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12207G>A , J01415.2:m.12207G>A GRCh38
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