Canonical Allele Identifier: PA2828555983
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 990600
ClinVar RCV Id: RCV001278658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Thr279Ser
CA4941398
NM_001374839.1:c.836C>G
CA372621134
NM_001374839.1:c.835A>T