Canonical Allele Identifier: CA120580

Gene:

Linked Data

• ClinVar Variation Id: 9617
• ClinVar RCV Id: RCV000010241 ; RCV000032996 ; RCV000495337 ; RCV000851098 ; RCV001089486
• dbSNP Id: rs121434453
• MyVariant Identifiers: chrMT:g.14709T>C (hg38)
• ERepo: CA120580/MONDO:0044970/014
• PubMed: PMID:4114165 ; PMID:7726154 ; PMID:7726155 ; PMID:9353617 ; PMID:10392369 ; PMID:11437868 ; PMID:12393175 ; PMID:15048886

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14709T>C , J01415.2:m.14709T>C	GRCh38