Canonical Allele Identifier: PA645395832
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 285046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg708Cys
CA2839605
NM_006005.3:c.2122C>T