Canonical Allele Identifier: CA120561
Gene:

Linked Data

ClinVar Variation Id: 9591
ClinVar RCV Id: RCV000010213 RCV000010214 RCV000850697 RCV003153298
dbSNP Id: rs199474659
MyVariant Identifiers: chrMT:g.3256C>T (hg38)
ERepo: CA120561/MONDO:0044970/014
PubMed: PMID:8254046 PMID:9506761
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3256C>T , J01415.2:m.3256C>T GRCh38
Search 100 bp 5'
Search 100 bp 3'