Canonical Allele Identifier: CA10581204
Gene:

Linked Data

ClinVar Variation Id: 235017
dbSNP Id: rs200009705
MyVariant Identifiers: chrMT:g.4363T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4363T>C , J01415.2:m.4363T>C GRCh38