Canonical Allele Identifier: PA2827289910
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 423698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317174.2:p.Gly62Arg
CA5975687
NM_001330245.2:c.184G>A
CA380309292
NM_001330245.2:c.184G>C