Canonical Allele Identifier: PA2829880048
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3544
ClinVar RCV Id: RCV000003722 RCV002512719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Arg70Cys
CA116339
NM_017767.3:c.208C>T