Canonical Allele Identifier: PA2826621381
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3538
ClinVar RCV Id: RCV000003716
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267486.1:p.Gly28Arg
CA116331
NM_001280557.2:c.82G>A
CA372618592
NM_001280557.2:c.82G>C