Allele Registry

Canonical Allele Identifier: CA254841

Gene:

Linked Data - Expert Curation

ClinGen Evidence Repository:

Classification Uncertain Significance

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.4295A>G

Linked Data - NCBI & NCI

ClinVar Allele:

24642

ClinVar RCV:

RCV000010226

RCV000022900

RCV000223744

RCV000224071

RCV000850718

ClinVar Variation:

9603

dbSNP:

121434467

Genomic Alleles

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

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