ClinGen Allele Registry
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Canonical Allele Identifier:
CA254838
Gene:
Linked Data
ClinVar Variation Id:
9587
ClinVar RCV Id:
RCV000010204
dbSNP Id:
rs121434463
MyVariant Identifiers:
chrMT:g.12320A>G (hg38)
PubMed:
PMID:9012410
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.12320A>G , J01415.2:m.12320A>G
GRCh38
Search 100 bp 5'
Search 100 bp 3'