Canonical Allele Identifier: CA131012
Gene:
ClinGen Classification:
Classification Uncertain Significance
Condition mitochondrial disease
VCEP Mitochondrial Diseases VCEP
ClinVar RCV:
RCV000035052
RCV000850891
ClinVar Variation:
42227
dbSNP:
111033319
MyVariant.info:
GRCh38 chrMT:g.7471del
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7471del , J01415.2:m.7471del GRCh38
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