Canonical Allele Identifier: PA2825788768
Gene: SLC39A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 218895
ClinVar RCV Id: RCV000203234 RCV001386978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128618.1:p.Gly38Arg
CA249424
NM_001135146.2:c.112G>C