Allele Registry

Canonical Allele Identifier: PA645395697

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000445526

RCV002488989

RCV002509070

ClinVar Variation:

393384

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Ala58Thr	CA16609249 NM_006005.3:c.172G>A