Canonical Allele Identifier: PA2828555982
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2607657
ClinVar RCV Id: RCV003357568
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Thr279Ile
CA372621133
NM_001374839.1:c.836C>T