Allele Registry

Canonical Allele Identifier: CA254837

Gene:

Linked Data - Expert Curation

ClinGen Evidence Repository:

Classification Likely Pathogenic

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.8313G>A

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010200

RCV003162233

ClinVar Variation:

9583

dbSNP:

118192101

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8313G>A , J01415.2:m.8313G>A	GRCh38

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