Canonical Allele Identifier: PA2742015171
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683148
ClinVar RCV Id: RCV003482015
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689477.3:p.Arg47Gly
CA5975676
NM_152264.5:c.139C>G