Canonical Allele Identifier: CA16603227

Gene:

Linked Data

• ClinVar Variation Id: 376983
• ClinVar RCV Id: RCV000426740 ; RCV000851017
• dbSNP Id: rs376606918
• MyVariant Identifiers: chrMT:g.12153C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12153C>T , J01415.2:m.12153C>T	GRCh38