Canonical Allele Identifier: PA1139700111
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg868Pro
CA91797871
NM_006005.3:c.2603G>C