Canonical Allele Identifier: PA2829880505
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164683
ClinVar RCV Id: RCV004461553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Ala383Thr
CA372619883
NM_017767.3:c.1147G>A