Canonical Allele Identifier: CA337099441
Gene:

Linked Data

ClinVar Variation Id: 690193
ClinVar RCV Id: RCV000851081 RCV002221590
dbSNP Id: rs2853498
MyVariant Identifiers: chrMT:g.12308A>G (hg38)
ERepo: CA337099441/MONDO:0044970/014
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12308A>G , J01415.2:m.12308A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'