Canonical Allele Identifier: PA2825920752
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Asp866Asn
CA182744
NM_001145853.1:c.2596G>A