Canonical Allele Identifier: PA658812782
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 499948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly212Arg
CA356172204
NM_006005.3:c.634G>C
CA356172205
NM_006005.3:c.634G>A