Allele Registry

Canonical Allele Identifier: PA136333

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000038638

RCV000269758

RCV000363867

RCV001523400

RCV002464096

ClinVar Variation:

45434

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg456His	CA136332 NM_006005.3:c.1367G>A