Allele Registry

Canonical Allele Identifier: PA2573099253

Gene: SLC39A13 HGNC NCBI

ClinVar Variation Id: 450588

HGVS (amino-acid)	Matching Registered Transcripts
NP_689477.3:p.Ser135Gly	CA5975754 NM_152264.5:c.403A>G