Canonical Allele Identifier: CA120585
Gene:

Linked Data

ClinVar Variation Id: 9622
ClinVar RCV Id: RCV000010247 RCV000010248 RCV000850838 RCV003162237
dbSNP Id: rs199476132
MyVariant Identifiers: chrMT:g.5728T>C (hg38)
ERepo: CA120585/MONDO:0044970/014
PubMed: PMID:16908752
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5728T>C , J01415.2:m.5728T>C GRCh38
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