ClinGen Allele Registry
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Canonical Allele Identifier:
PA916056182
Gene: SLC39A4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000359976
RCV000455765
RCV001515873
ClinVar Variation:
362260
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_060237.3:p.Ala89Thr
CA4941734
NM_017767.3:c.265G>A