Canonical Allele Identifier: PA2829880476
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362236
ClinVar RCV Id: RCV000312232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Glu367Gln
CA4941332
NM_017767.3:c.1099G>C