Canonical Allele Identifier: PA2580517421
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2045129
ClinVar RCV Id: RCV002917950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689477.3:p.Ser55Pro
CA380309209
NM_152264.5:c.163T>C