Canonical Allele Identifier: PA916060312
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3537
ClinVar RCV Id: RCV000003715 RCV001042457 RCV003415640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Pro200Leu
CA116329
NM_130849.4:c.599C>T