Canonical Allele Identifier: CA120550
Gene:

Linked Data

ClinVar Variation Id: 9572
ClinVar RCV Id: RCV000010185 RCV000851158
dbSNP Id: rs199474701
MyVariant Identifiers: chrMT:g.15967G>A (hg38)
PubMed: PMID:19273760 PMID:20301693
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15967G>A , J01415.2:m.15967G>A GRCh38
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