Canonical Allele Identifier: CA254847
Gene:

Linked Data

ClinVar Variation Id: 9632
ClinVar RCV Id: RCV000010262 RCV000010263 RCV000722075
dbSNP Id: rs267606619
MyVariant Identifiers: chrMT:g.1494C>T (hg38)
ERepo: CA254847/MONDO:0044970/014
PubMed: PMID:14681830 PMID:16380089 PMID:17085680 PMID:17434445 PMID:17698030 PMID:17698299 PMID:18830133 PMID:19682603 PMID:20100600 PMID:20416460 PMID:22992668 PMID:25515069 PMID:27397648
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1494C>T , J01415.2:m.1494C>T GRCh38
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