Canonical Allele Identifier: PA2741923603
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2808359
ClinVar RCV Id: RCV003684810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Leu567_Phe568dup
CA2669843448
NM_006005.3:c.1698_1703dup
CA2669843449
NM_006005.3:c.1699_1704dup