Canonical Allele Identifier: CA259739

Gene:

Linked Data

• ClinVar Variation Id: 30001
• ClinVar RCV Id: RCV000022896 ; RCV000506681 ; RCV003319171
• dbSNP Id: rs200077222
• MyVariant Identifiers: chrMT:g.5814T>C (hg38)
• ERepo: CA259739/MONDO:0044970/014
• PubMed: PMID:8829635 ; PMID:9185178

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5814T>C , J01415.2:m.5814T>C	GRCh38