Allele Registry

Canonical Allele Identifier: CA120541

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.5537_5538insT

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010164

RCV000010165

RCV001268092

ClinVar Variation:

9555

dbSNP:

199474672

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5537_5538insT , J01415.2:m.5537_5538insT	GRCh38

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