Allele Registry

Canonical Allele Identifier: PA2826621381

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000003716

ClinVar Variation:

3538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001267486.1:p.Gly28Arg	CA116331 NM_001280557.2:c.82G>A CA372618592 NM_001280557.2:c.82G>C