Allele Registry

Canonical Allele Identifier: PA916060307

Gene: SLC39A4 HGNC NCBI

ClinVar Allele:

18583

ClinVar RCV:

RCV000003722

RCV002512719

ClinVar Variation:

3544

HGVS (amino-acid)	Matching Registered Transcripts
NP_570901.3:p.Arg95Cys	CA116339 NM_130849.4:c.283C>T