Canonical Allele Identifier: PA2829880439
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3539
ClinVar RCV Id: RCV000003717 RCV001851627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Gly349Arg
CA116333
NM_017767.3:c.1045G>A
CA372621131
NM_017767.3:c.1045G>C