Canonical Allele Identifier: CA120572
Gene:

Linked Data

ClinVar Variation Id: 9605
ClinVar RCV Id: RCV000010228 RCV000850717
dbSNP Id: rs121434469
MyVariant Identifiers: chrMT:g.4290T>C (hg38)
PubMed: PMID:15121771
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4290T>C , J01415.2:m.4290T>C GRCh38
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