Allele Registry

Canonical Allele Identifier: PA2825920150

Gene: WFS1 HGNC NCBI

ClinVar Variation Id: 2794872

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Phe516Leu	CA356175902 NM_001145853.1:c.1546T>C CA356175911 NM_001145853.1:c.1548C>A CA356175913 NM_001145853.1:c.1548C>G