Canonical Allele Identifier: PA2825920179
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 137914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Pro533Ser
CA232537
NM_001145853.1:c.1597C>T