Allele Registry

Canonical Allele Identifier: PA182615

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000155337

ClinVar Variation:

178588

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Val333Phe	CA182614 NM_006005.3:c.997G>T