Canonical Allele Identifier: PA2830292946
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371385
ClinVar RCV Id: RCV001878974 RCV004040522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689477.3:p.Arg341His
CA5976051
NM_152264.5:c.1022G>A