WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Canonical Allele Identifier:
CA120568
Gene:
Linked Data
ClinVar Variation Id:
9598
dbSNP Id:
rs199474666
MyVariant Identifiers:
chrMT:g.3274A>G (hg38)
PubMed:
PMID:11723298
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3274A>G , J01415.2:m.3274A>G | GRCh38 |