Canonical Allele Identifier: PA2825788796
Gene: SLC39A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 871104
ClinVar RCV Id: RCV001090879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128618.1:p.Phe203Ser
CA357753412
NM_001135146.2:c.608T>C