ClinGen Allele Registry
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Canonical Allele Identifier:
CA120584
Gene:
Linked Data
ClinVar Variation Id:
9621
ClinVar RCV Id:
RCV000010246
dbSNP Id:
rs199476131
MyVariant Identifiers:
chrMT:g.5692T>C (hg38)
PubMed:
PMID:7980504
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.5692T>C , J01415.2:m.5692T>C
GRCh38
Search 100 bp 5'
Search 100 bp 3'