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:
CA337099405
Gene:
Linked Data
ClinVar Variation Id:
690137
ClinVar RCV Id:
RCV000851019
dbSNP Id:
rs386829147
MyVariant Identifiers:
chrMT:g.12161T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12161T>C , J01415.2:m.12161T>C | GRCh38 |