Canonical Allele Identifier: CA120561

Gene:

Linked Data

• ClinVar Variation Id: 9591
• ClinVar RCV Id: RCV000010213 ; RCV000010214 ; RCV000850697 ; RCV003153298
• dbSNP Id: rs199474659
• MyVariant Identifiers: chrMT:g.3256C>T (hg38)
• ERepo: CA120561/MONDO:0044970/014
• PubMed: PMID:8254046 ; PMID:9506761

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3256C>T , J01415.2:m.3256C>T	GRCh38