Allele Registry

Canonical Allele Identifier: CA259739

Gene:

Linked Data - Expert Curation

ClinGen Evidence Repository:

Classification Likely Benign

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.5814T>C

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000022896

RCV000506681

RCV003319171

ClinVar Variation:

30001

dbSNP:

200077222

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5814T>C , J01415.2:m.5814T>C	GRCh38

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