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)
PubMed: PMID:4114165 PMID:7726154 PMID:7726155 PMID:9353617 PMID:10392369 PMID:11437868 PMID:12393175 PMID:15048886
ERepo: CA120580/MONDO:0044970/014
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14709T>C , J01415.2:m.14709T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'