Canonical Allele Identifier: PA325021
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg732Cys
CA325020
NM_006005.3:c.2194C>T