Canonical Allele Identifier: CA120581
Gene:

Linked Data

ClinVar Variation Id: 9618
ClinVar RCV Id: RCV000010243 RCV000224954 RCV000495655 RCV000851087
dbSNP Id: rs387906421
MyVariant Identifiers: chrMT:g.14674T>C (hg38)
ERepo: CA120581/MONDO:0044970/014
PubMed: PMID:19720722 PMID:21194154 PMID:21931168
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14674T>C , J01415.2:m.14674T>C GRCh38
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