Allele Registry

Canonical Allele Identifier: PA2829880281

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000954694

ClinVar Variation:

774671

HGVS (amino-acid)	Matching Registered Transcripts
NP_060237.3:p.Arg226Trp	CA187649376 NM_017767.3:c.676C>T