Canonical Allele Identifier: PA916060346
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362236
ClinVar RCV Id: RCV000312232
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Glu392Gln
CA4941332
NM_130849.4:c.1174G>C