Canonical Allele Identifier: CA337097836
Gene:

Linked Data

ClinVar Variation Id: 690067
ClinVar RCV Id: RCV000850941
dbSNP Id: rs371589230
MyVariant Identifiers: chrMT:g.8311T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8311T>C , J01415.2:m.8311T>C GRCh38