Canonical Allele Identifier: CA16040645

Gene:

Linked Data

• ClinVar Variation Id: 370045
• ClinVar RCV Id: RCV000408925 ; RCV000408928 ; RCV000408938 ; RCV000408950 ; RCV000850706
• dbSNP Id: rs1057516057
• MyVariant Identifiers: chrMT:g.3275C>T (hg38)
• PubMed: PMID:28027978

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3275C>T , J01415.2:m.3275C>T	GRCh38