Allele Registry

Canonical Allele Identifier: PA136341

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000038646

RCV000339307

RCV000404430

RCV000987411

RCV001523401

RCV003075593

ClinVar Variation:

45442

2156690

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg611His	CA136340 NM_006005.3:c.1832G>A CA2580071779 NM_006005.3:c.1832_1833delinsAT