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)

Genomic Alleles

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