Canonical Allele Identifier: PA2825667307
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 423698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Gly62Arg
CA5975687
NM_001128225.3:c.184G>A
CA380309292
NM_001128225.3:c.184G>C