Canonical Allele Identifier: CA120546
Gene:

Linked Data

ClinVar Variation Id: 9562
ClinVar RCV Id: RCV000010174 RCV000010175 RCV000850907 RCV002247286
dbSNP Id: rs199474817
MyVariant Identifiers: chrMT:g.7512T>C (hg38)
PubMed: PMID:7669057 PMID:9832034
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7512T>C , J01415.2:m.7512T>C GRCh38
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