Canonical Allele Identifier: PA2828555967
Gene: SLC39A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 990601
ClinVar RCV Id: RCV001278659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361768.1:p.Val262Phe
CA372621237
NM_001374839.1:c.784G>T