Canonical Allele Identifier: CA120588
Gene:

Linked Data

ClinVar Variation Id: 9626
ClinVar RCV Id: RCV000010252
dbSNP Id: rs199474823
MyVariant Identifiers: chrMT:g.2991T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.2991T>C , J01415.2:m.2991T>C GRCh38