Canonical Allele Identifier: CA120569
Gene:

Linked Data

ClinVar Variation Id: 9601
ClinVar RCV Id: RCV000010224 RCV000850729
dbSNP Id: rs121434465
MyVariant Identifiers: chrMT:g.4317A>G (hg38)
PubMed: PMID:1978914 PMID:12621050
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4317A>G , J01415.2:m.4317A>G GRCh38
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