Allele Registry

Canonical Allele Identifier: CA913182452

Gene:

Linked Data - Expert Curation

ClinGen Evidence Repository:

Classification Uncertain Significance

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000850967

ClinVar Variation:

690090

dbSNP:

121434475

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.9997T>A , J01415.2:m.9997T>A	GRCh38

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