Canonical Allele Identifier: PA916060328
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362242
ClinVar Variation Id: 1084509
ClinVar RCV Id: RCV001401580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Thr357Ala
CA4941409
NM_130849.4:c.1069A>G
CA2499219171
NM_130849.4:c.1068_1069delinsTG