Canonical Allele Identifier: PA2829880768
Gene: SLC39A4 HGNC NCBI
ClinVar RCV:
RCV000003716
ClinVar Variation:
3538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Gly501Arg
CA116331
NM_017767.3:c.1501G>A
CA372618592
NM_017767.3:c.1501G>C