Canonical Allele Identifier: PA2829880373
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2461345
ClinVar RCV Id: RCV003196273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Tyr304Ser
CA4941435
NM_017767.3:c.911A>C