Canonical Allele Identifier: PA2742008416
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_570901.3:p.Thr373Ile
CA372621133
NM_130849.4:c.1118C>T