Allele Registry

Canonical Allele Identifier: CA254829

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.5888del

GRCh38 chrMT:g.5885del

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010160

ClinVar Variation:

9551

dbSNP:

118203892

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5888del , J01415.2:m.5888del	GRCh38

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