Canonical Allele Identifier: PA2825920348
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Thr628Met
CA2839533
NM_001145853.1:c.1883C>T