Canonical Allele Identifier: CA337098660
Gene:

Linked Data

ClinVar Variation Id: 690095
ClinVar RCV Id: RCV000850972
dbSNP Id: rs201906571
MyVariant Identifiers: chrMT:g.10007T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10007T>C , J01415.2:m.10007T>C GRCh38