Allele Registry

Canonical Allele Identifier: PA136364

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000038668

RCV000259675

RCV001157248

RCV001414831

RCV001523396

RCV002464100

RCV002496615

ClinVar Variation:

45463

1094353

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Val333Ile	CA136363 NM_006005.3:c.997G>A CA2499217321 NM_006005.3:c.996_997delinsAA