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:
CA120556
Gene:
Linked Data
ClinVar Variation Id:
9582
dbSNP Id:
rs118192103
MyVariant Identifiers:
chrMT:g.8342G>A (hg38)
PubMed:
PMID:10220860
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8342G>A , J01415.2:m.8342G>A | GRCh38 |