Allele Registry

Canonical Allele Identifier: PA2825920560

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000191145

RCV001852540

ClinVar Variation:

209206

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Cys755Arg	CA276183 NM_001145853.1:c.2263T>C