Allele Registry

Canonical Allele Identifier: PA2829880232

Gene: SLC39A4 HGNC NCBI

ClinVar RCV:

RCV000003715

RCV001042457

RCV003415640

ClinVar Variation:

3537

HGVS (amino-acid)	Matching Registered Transcripts
NP_060237.3:p.Pro175Leu	CA116329 NM_017767.3:c.524C>T