Canonical Allele Identifier: PA2830186137
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164683
ClinVar RCV Id: RCV004461553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Ala408Thr
CA372619883
NM_130849.4:c.1222G>A