Canonical Allele Identifier: CA130997

Gene:

Linked Data

• ClinVar Variation Id: 42210
• ClinVar RCV Id: RCV000035035
• dbSNP Id: rs111033320
• MyVariant Identifiers: chrMT:g.1187T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1187T>C , J01415.2:m.1187T>C	GRCh38