Canonical Allele Identifier: PA105464
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372583
ClinVar RCV Id: RCV000413912 RCV002469144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala126Thr
CA2838877
NM_001145853.1:c.376G>A