Allele Registry

Canonical Allele Identifier: CA131013

Gene:

Linked Data

ClinGen Classification:

Classification Benign

Condition mitochondrial disease

VCEP Mitochondrial Diseases VCEP

ClinVar RCV:

RCV000035053

RCV000850894

RCV002221482

ClinVar Variation:

42228

dbSNP:

201950015

MyVariant.info:

GRCh38 chrMT:g.7476C>T

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7476C>T , J01415.2:m.7476C>T	GRCh38

Search 100 bp 5'

Search 100 bp 3'