Canonical Allele Identifier: PA2825667312
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Gly74Asp
CA115360
NM_001128225.3:c.221G>A