Canonical Allele Identifier: CA344658
Gene:

Linked Data

ClinVar Variation Id: 42212
dbSNP Id: rs28358572
MyVariant Identifiers: chrMT:g.1243T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1243T>C , J01415.2:m.1243T>C GRCh38