Canonical Allele Identifier: PA2825920757
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1207795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg868Cys
CA2839800
NM_001145853.1:c.2602C>T