Canonical Allele Identifier: PA2828689535
Gene: SLC30A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 375609
ClinVar RCV Id: RCV000417081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363858.1:p.His273Tyr
CA1399182
NM_001376929.1:c.817C>T