Canonical Allele Identifier: PA2825497815
Gene: SLC39A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164720
ClinVar RCV Id: RCV004461590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092876.1:p.Pro258Leu
CA8939041
NM_001099406.2:c.773C>T