Allele Registry

Canonical Allele Identifier: PA259832

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV003778168

ClinVar Variation:

2627560

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Val707Phe	CA259830 NM_006005.3:c.2119G>T