Canonical Allele Identifier: CA337096487

Gene:

Linked Data

• ClinVar Variation Id: 223247
• ClinVar RCV Id: RCV000850711 ; RCV002291215
• dbSNP Id: rs869312463
• MyVariant Identifiers: chrMT:g.3291T>C (hg38)
• ERepo: CA337096487/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3291T>C , J01415.2:m.3291T>C	GRCh38