Canonical Allele Identifier: PA2828556002
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 762895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Arg308Cys
CA4941328
NM_001374839.1:c.922C>T