Canonical Allele Identifier: CA120564
Gene:

Linked Data

ClinVar Variation Id: 9594
ClinVar RCV Id: RCV000010217 RCV000850692
dbSNP Id: rs199474661
MyVariant Identifiers: chrMT:g.3252A>G (hg38)
PubMed: PMID:8111377
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3252A>G , J01415.2:m.3252A>G GRCh38
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