Canonical Allele Identifier: PA2828556007
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 910707
ClinVar RCV Id: RCV001162686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Gly315Arg
CA372619857
NM_001374839.1:c.943G>C
CA372619859
NM_001374839.1:c.943G>A