Canonical Allele Identifier: CA658653720
Gene:

Linked Data

ClinVar Variation Id: 441156
dbSNP Id: rs1556423009
MyVariant Identifiers: chrMT:g.5561T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5561T>C , J01415.2:m.5561T>C GRCh38