Canonical Allele Identifier: PA2825920222
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 427051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg558His
CA2839440
NM_001145853.1:c.1673G>A