Allele Registry

Canonical Allele Identifier: PA105738

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000503566

RCV001849390

RCV001857186

RCV002506232

RCV003233655

RCV003335435

ClinVar Variation:

437297

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Pro885Leu	CA2839823 NM_001145853.1:c.2654C>T