Canonical Allele Identifier: CA120576
Gene:

Linked Data

ClinVar Variation Id: 9610
ClinVar RCV Id: RCV000010234 RCV000851013 RCV002247294
dbSNP Id: rs121434474
MyVariant Identifiers: chrMT:g.12147G>A (hg38)
PubMed: PMID:14967777 PMID:15111688
ERepo: CA120576/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12147G>A , J01415.2:m.12147G>A GRCh38
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