Canonical Allele Identifier: PA2825920696
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 95324
ClinVar RCV Id: RCV000081341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Gly834Ser
CA222903
NM_001145853.1:c.2500G>A