Canonical Allele Identifier: PA232538
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 137914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Pro533Ser
CA232537
NM_006005.3:c.1597C>T