Canonical Allele Identifier: PA2825920239
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2808359
ClinVar RCV Id: RCV003684810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Leu567_Phe568dup
CA2669843448
NM_001145853.1:c.1698_1703dup
CA2669843449
NM_001145853.1:c.1699_1704dup