Canonical Allele Identifier: PA2742008414
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2509531
ClinVar RCV Id: RCV003250864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570901.3:p.Gly330Ser
CA4941433
NM_130849.4:c.988G>A