Allele Registry

Canonical Allele Identifier: PA916060324

Gene: SLC39A4 HGNC NCBI

ClinVar Allele:

18581

ClinVar RCV:

RCV000003720

ClinVar Variation:

3542

HGVS (amino-acid)	Matching Registered Transcripts
NP_570901.3:p.Gly330Asp	CA116337 NM_130849.4:c.989G>A