Allele Registry

Canonical Allele Identifier: CA340926

Gene:

Linked Data - Expert Curation

ClinGen Evidence Repository:

Classification Benign

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.4336T>C

Linked Data - NCBI & NCI

ClinVar Allele:

24654

ClinVar RCV:

RCV000010239

RCV000224964

RCV000850736

RCV001288305

ClinVar Variation:

9615

dbSNP:

41456348

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4336T>C , J01415.2:m.4336T>C	GRCh38

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