Canonical Allele Identifier: PA2825667345
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 450588
ClinVar RCV Id: RCV000520437 RCV001213714 RCV002279315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Ser135Gly
CA5975754
NM_001128225.3:c.403A>G