Allele Registry

Canonical Allele Identifier: PA2825920220

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV002664337

ClinVar Variation:

2203524

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Leu557Phe	CA2839436 NM_001145853.1:c.1669C>T