ClinGen Allele Registry
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Canonical Allele Identifier:
CA259739
Gene:
Linked Data
ClinVar Variation Id:
30001
ClinVar RCV Id:
RCV000022896
RCV000506681
RCV003319171
dbSNP Id:
rs200077222
MyVariant Identifiers:
chrMT:g.5814T>C (hg38)
PubMed:
PMID:8829635
PMID:9185178
ERepo:
CA259739/MONDO:0044970/014
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.5814T>C , J01415.2:m.5814T>C
GRCh38
Search 100 bp 5'
Search 100 bp 3'