Canonical Allele Identifier: PA916060372
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_570901.3:p.Gly526Arg
CA116331
NM_130849.4:c.1576G>A
CA372618592
NM_130849.4:c.1576G>C