Canonical Allele Identifier: PA1139720200
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 907358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg232His
CA2838997
NM_006005.3:c.695G>A