Canonical Allele Identifier: CA120562
Gene:

Linked Data

ClinVar Variation Id: 9592
dbSNP Id: rs199474660
MyVariant Identifiers: chrMT:g.3303C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3303C>T , J01415.2:m.3303C>T GRCh38