Canonical Allele Identifier: PA2825919900
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 452350
ClinVar Variation Id: 1966944
ClinVar RCV Id: RCV002721671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Phe374Leu
CA356174298
NM_001145853.1:c.1120T>C
CA356174303
NM_001145853.1:c.1122C>A
CA356174304
NM_001145853.1:c.1122C>G