Canonical Allele Identifier: PA2825667445
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164661
ClinVar RCV Id: RCV004461531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Ala358Val
CA380315489
NM_001128225.3:c.1073C>T