Canonical Allele Identifier: PA2825919920
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Glu385Lys
CA295789
NM_001145853.1:c.1153G>A