Canonical Allele Identifier: PA182745
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Asp866Asn
CA182744
NM_006005.3:c.2596G>A