Canonical Allele Identifier: PA2825919977
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Phe413Val
CA179641
NM_001145853.1:c.1237T>G