Canonical Allele Identifier: CA120574
Gene:

Linked Data

ClinVar Variation Id: 9608
ClinVar RCV Id: RCV000010231 RCV000010232 RCV000851036
dbSNP Id: rs3134560
MyVariant Identifiers: chrMT:g.12192G>A (hg38)
PubMed: PMID:11038324 PMID:12560876
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12192G>A , J01415.2:m.12192G>A GRCh38
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