Canonical Allele Identifier: PA2829880340
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3545
ClinVar RCV Id: RCV000003723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Gln278His
CA116341
NM_017767.3:c.834G>C
CA372621774
NM_017767.3:c.834G>T