Canonical Allele Identifier: CA337098849
Gene:

Linked Data

ClinVar Variation Id: 690128
ClinVar RCV Id: RCV000851008
dbSNP Id: rs28358279
MyVariant Identifiers: chrMT:g.10463T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10463T>C , J01415.2:m.10463T>C GRCh38