Canonical Allele Identifier: CA120570
Gene:

Linked Data

ClinVar Variation Id: 9602
ClinVar RCV Id: RCV000010225 RCV002247291
dbSNP Id: rs121434466
MyVariant Identifiers: chrMT:g.4269A>G (hg38)
PubMed: PMID:1632786
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4269A>G , J01415.2:m.4269A>G GRCh38
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