Allele Registry

Canonical Allele Identifier: CA337099441

Gene:

Linked Data

ClinGen Classification:

Classification Benign

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

ClinVar RCV:

RCV000851081

RCV002221590

ClinVar Variation:

690193

dbSNP:

2853498

MyVariant.info:

GRCh38 chrMT:g.12308A>G

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12308A>G , J01415.2:m.12308A>G	GRCh38

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