Canonical Allele Identifier: CA120552

Gene:

Linked Data

• ClinVar Variation Id: 9576
• ClinVar RCV Id: RCV000010189 ; RCV000850644 ; RCV001804724 ; RCV002247290
• dbSNP Id: rs387906420
• MyVariant Identifiers: chrMT:g.616T>C (hg38)
• ERepo: CA120552/MONDO:0044970/014
• PubMed: PMID:20142618

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.616T>C , J01415.2:m.616T>C	GRCh38