Canonical Allele Identifier: CA340926
Gene:

Linked Data

ClinVar Variation Id: 9615
ClinVar RCV Id: RCV000010239 RCV000224964 RCV000850736 RCV001288305
dbSNP Id: rs41456348
MyVariant Identifiers: chrMT:g.4336T>C (hg38)
ERepo: CA340926/MONDO:0044970/014
PubMed: PMID:11424923
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4336T>C , J01415.2:m.4336T>C GRCh38
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