Canonical Allele Identifier: CA340926
Gene:

Linked Data

ClinVar Variation Id: 9615
dbSNP Id: rs41456348
MyVariant Identifiers: chrMT:g.4336T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4336T>C , J01415.2:m.4336T>C GRCh38