Canonical Allele Identifier: PA2825788951
Gene: SLC39A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 218897
ClinVar RCV Id: RCV000203248 RCV000733882 RCV003226248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128620.1:p.Gly137Cys
CA249426
NM_001135148.2:c.409G>T