Canonical Allele Identifier: PA2828556006
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164684
ClinVar RCV Id: RCV004461554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Gly315Glu
CA372619853
NM_001374839.1:c.944G>A