Allele Registry

Canonical Allele Identifier: PA645395805

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000445427

RCV001851112

RCV002026196

RCV003128192

ClinVar Variation:

393390

1513489

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Met632Ile	CA16609253 NM_006005.3:c.1896G>T CA356177057 NM_006005.3:c.1896G>A CA356177058 NM_006005.3:c.1896G>C