Canonical Allele Identifier: PA645395884
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 287170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Cys850Tyr
CA2839773
NM_006005.3:c.2549G>A