Allele Registry

Canonical Allele Identifier: PA105756

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000004780

RCV000238945

RCV001851653

ClinVar Variation:

4522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Thr699Met	CA253201 NM_001145853.1:c.2096C>T