Canonical Allele Identifier: CA337098838
Gene:

Linked Data

ClinVar Variation Id: 690122
ClinVar RCV Id: RCV000851002
dbSNP Id: rs878874133
MyVariant Identifiers: chrMT:g.10454T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10454T>C , J01415.2:m.10454T>C GRCh38