Canonical Allele Identifier: CA120543

Gene:

Linked Data

• ClinVar Variation Id: 9558
• ClinVar RCV Id: RCV000010168
• dbSNP Id: rs387906418
• MyVariant Identifiers: chrMT:g.5545C>T (hg38)
• PubMed: PMID:18337306
• ERepo: CA120543/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5545C>T , J01415.2:m.5545C>T	GRCh38