Allele Registry

Canonical Allele Identifier: PA916060372

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000003716

ClinVar Variation:

3538

HGVS (amino-acid)	Matching Registered Transcripts
NP_570901.3:p.Gly526Arg	CA116331 NM_130849.4:c.1576G>A CA372618592 NM_130849.4:c.1576G>C