Allele Registry

Canonical Allele Identifier: CA120582

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.7526A>G

Linked Data - NCBI & NCI

ClinVar Allele:

24658

ClinVar RCV:

RCV000010244

ClinVar Variation:

9619

dbSNP:

121434454

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7526A>G , J01415.2:m.7526A>G	GRCh38

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