Allele Registry

Canonical Allele Identifier: PA105727

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000004767

RCV000756934

ClinVar Variation:

4509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Pro724Leu	CA253184 NM_001145853.1:c.2171C>T