Canonical Allele Identifier: PA323354
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215370
ClinVar RCV Id: RCV000198824 RCV001152301 RCV001152302 RCV001722100 RCV003147401 RCV004530177 RCV002517277
ClinVar Variation Id: 2125078
ClinVar RCV Id: RCV003057479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe783Leu
CA323353
NM_006005.3:c.2347T>C
CA356178415
NM_006005.3:c.2349C>A
CA356178416
NM_006005.3:c.2349C>G