Canonical Allele Identifier: PA2830292955
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_689477.3:p.Ala351Val
CA380315489
NM_152264.5:c.1052C>T