Allele Registry

Canonical Allele Identifier: PA2828555835

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000330943

RCV000454589

RCV001515874

ClinVar Variation:

362265

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361768.1:p.Ala58Thr	CA4941845 NM_001374839.1:c.172G>A