Canonical Allele Identifier: PA2825919704
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1189682
ClinVar RCV Id: RCV001550129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ser238Pro
CA356172362
NM_001145853.1:c.712T>C