Canonical Allele Identifier: PA2829880437
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2607657
ClinVar RCV Id: RCV003357568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Thr348Ile
CA372621133
NM_017767.3:c.1043C>T