Allele Registry

Canonical Allele Identifier: CA120573

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.4291T>C

Linked Data - NCBI & NCI

ClinVar Allele:

24646

ClinVar RCV:

RCV000010230

ClinVar Variation:

9607

dbSNP:

121434471

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4291T>C , J01415.2:m.4291T>C	GRCh38

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