Canonical Allele Identifier: CA254841
Gene:

Linked Data

ClinVar Variation Id: 9603
ClinVar RCV Id: RCV000010226 RCV000022900 RCV000223744 RCV000224071 RCV000850718
dbSNP Id: rs121434467
MyVariant Identifiers: chrMT:g.4295A>G (hg38)
PubMed: PMID:8889580 PMID:22241583
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4295A>G , J01415.2:m.4295A>G GRCh38
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