Allele Registry

Canonical Allele Identifier: PA916060316

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000954694

ClinVar Variation:

774671

HGVS (amino-acid)	Matching Registered Transcripts
NP_570901.3:p.Arg251Trp	CA187649376 NM_130849.4:c.751C>T