Canonical Allele Identifier: CA130999
Gene:

Linked Data

ClinVar Variation Id: 42213
ClinVar RCV Id: RCV000035038
dbSNP Id: rs111033354
MyVariant Identifiers: chrMT:g.1310C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1310C>T , J01415.2:m.1310C>T GRCh38