Canonical Allele Identifier: CA10581333
Gene:

Linked Data

ClinVar Variation Id: 235498
dbSNP Id: rs878853053
MyVariant Identifiers: chrMT:g.5553T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5553T>C , J01415.2:m.5553T>C GRCh38