Canonical Allele Identifier: PA2828555946
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2509531
ClinVar RCV Id: RCV003250864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Gly236Ser
CA4941433
NM_001374839.1:c.706G>A