Canonical Allele Identifier: PA2573183031
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371385
ClinVar RCV Id: RCV001878974 RCV004040522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Arg348His
CA5976051
NM_001128225.3:c.1043G>A