Canonical Allele Identifier: CA270624
Gene:

Linked Data

ClinVar Variation Id: 143902
ClinVar RCV Id: RCV000133441 RCV000851131
dbSNP Id: rs193303002
MyVariant Identifiers: chrMT:g.15927G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15927G>A , J01415.2:m.15927G>A GRCh38
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