Canonical Allele Identifier: CA254829
Gene:

Linked Data

ClinVar Variation Id: 9551
ClinVar RCV Id: RCV000010160
dbSNP Id: rs118203892
MyVariant Identifiers: chrMT:g.5888del (hg38) chrMT:g.5885del (hg38)
PubMed: PMID:11756614
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Genomic Alleles

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