Allele Registry

Canonical Allele Identifier: CA913163293

Gene:

Linked Data - Expert Curation

ClinGen Evidence Repository:

Classification Uncertain Significance

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000850670

RCV003153871

ClinVar Variation:

689840

dbSNP:

1603218588

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1630A>G , J01415.2:m.1630A>G	GRCh38

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