Canonical Allele Identifier: PA322172
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly76Val
CA322171
NM_006005.3:c.227G>T