Canonical Allele Identifier: CA254835
Gene:

Linked Data

ClinVar Variation Id: 9578
ClinVar RCV Id: RCV000010191
dbSNP Id: rs118203884
MyVariant Identifiers: chrMT:g.4409T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4409T>C , J01415.2:m.4409T>C GRCh38