Canonical Allele Identifier: PA2829880384
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2306803
ClinVar RCV Id: RCV002879188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Thr309Met
CA4941430
NM_017767.3:c.926C>T