Allele Registry

Canonical Allele Identifier: PA2825919780

Gene: WFS1 HGNC NCBI

ClinVar Allele:

1306556

ClinVar RCV:

RCV001768179

ClinVar Variation:

1317613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Leu303Pro	CA356173863 NM_001145853.1:c.908T>C