Canonical Allele Identifier: CA131013
Gene:

Linked Data

ClinVar Variation Id: 42228
ClinVar RCV Id: RCV000035053 RCV000850894 RCV002221482
dbSNP Id: rs201950015
MyVariant Identifiers: chrMT:g.7476C>T (hg38)
PubMed: PMID:8155739 PMID:8728705 PMID:9384601 PMID:15286157 PMID:18790089 PMID:19371214 PMID:21621438
ERepo: CA131013/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7476C>T , J01415.2:m.7476C>T GRCh38
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