Canonical Allele Identifier: PA2825920172
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2203522
ClinVar RCV Id: RCV002651810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Tyr528His
CA2839411
NM_001145853.1:c.1582T>C