Canonical Allele Identifier: PA658812767
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 517251

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg146Cys
CA356171734
NM_006005.3:c.436C>T