Canonical Allele Identifier: PA2829880414
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 362242
ClinVar RCV Id: RCV000305246 RCV000454515 RCV001520476
ClinVar Variation Id: 1084509
ClinVar RCV Id: RCV001401580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060237.3:p.Thr332Ala
CA4941409
NM_017767.3:c.994A>G
CA2499219171
NM_017767.3:c.993_994delinsTG