Canonical Allele Identifier: CA176741
Gene:

Linked Data

ClinVar Variation Id: 163983
ClinVar RCV Id: RCV000151027
dbSNP Id: rs727503163
MyVariant Identifiers: chrMT:g.1040T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1040T>C , J01415.2:m.1040T>C GRCh38