Canonical Allele Identifier: PA916060350
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362235
ClinVar RCV Id: RCV000406648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Ala412Thr
CA4941321
NM_130849.4:c.1234G>A