Canonical Allele Identifier: CA185274

Gene:

Linked Data

• ClinVar Variation Id: 179852
• ClinVar RCV Id: RCV000156652
• dbSNP Id: rs727505171
• MyVariant Identifiers: chrMT:g.1120C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1120C>T , J01415.2:m.1120C>T	GRCh38