Canonical Allele Identifier: CA120548
Gene:

Linked Data

ClinVar Variation Id: 9569
ClinVar RCV Id: RCV000010182 RCV000850901 RCV002247288 RCV003319162
dbSNP Id: rs387906419
MyVariant Identifiers: chrMT:g.7497G>A (hg38)
PubMed: PMID:14605505
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7497G>A , J01415.2:m.7497G>A GRCh38
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