Canonical Allele Identifier: PA2825919972
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val412Asp
CA2839277
NM_001145853.1:c.1235T>A