Allele Registry

Canonical Allele Identifier: PA2829880376

Gene: SLC39A4 HGNC NCBI

ClinVar Allele:

18581

ClinVar RCV:

RCV000003720

ClinVar Variation:

3542

HGVS (amino-acid)	Matching Registered Transcripts
NP_060237.3:p.Gly305Asp	CA116337 NM_017767.3:c.914G>A