Canonical Allele Identifier: PA2828555950
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2306803
ClinVar RCV Id: RCV002879188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Thr240Met
CA4941430
NM_001374839.1:c.719C>T