Canonical Allele Identifier: CA120541
Gene:

Linked Data

ClinVar Variation Id: 9555
ClinVar RCV Id: RCV000010164 RCV000010165 RCV001268092
dbSNP Id: rs199474672
MyVariant Identifiers: chrMT:g.5537_5538insT (hg38)
PubMed: PMID:9266739 PMID:12776230 PMID:20301352
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Genomic Alleles

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