Allele Registry

Canonical Allele Identifier: PA2828555899

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000954694

ClinVar Variation:

774671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361768.1:p.Arg157Trp	CA187649376 NM_001374839.1:c.469C>T