Canonical Allele Identifier: PA2828555968
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362242
ClinVar Variation Id: 1084509
ClinVar RCV Id: RCV001401580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Thr263Ala
CA4941409
NM_001374839.1:c.787A>G
CA2499219171
NM_001374839.1:c.786_787delinsTG