Canonical Allele Identifier: CA337098672
Gene:

Linked Data

ClinVar Variation Id: 690104
dbSNP Id: rs41347846
MyVariant Identifiers: chrMT:g.10034T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10034T>C , J01415.2:m.10034T>C GRCh38