Canonical Allele Identifier: PA645480268
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_061183.2:p.His336Tyr
CA1399182
NM_018713.3:c.1006C>T