Allele Registry

Canonical Allele Identifier: PA295802

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000155411

RCV000351887

RCV000415767

RCV000445544

RCV000987408

RCV001157342

ClinVar Variation:

137913

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Leu432Val	CA295801 NM_006005.3:c.1294C>G