Canonical Allele Identifier: CA170534
Gene:

Linked Data

ClinVar Variation Id: 143905
ClinVar RCV Id: RCV000133444 RCV000851148
dbSNP Id: rs527236200
MyVariant Identifiers: chrMT:g.15943T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15943T>C , J01415.2:m.15943T>C GRCh38
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