Canonical Allele Identifier: PA2825919418
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 252656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala57Thr
CA2838810
NM_001145853.1:c.169G>A