Canonical Allele Identifier: PA2825920132
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2710025
ClinVar RCV Id: RCV003550240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Cys505Gly
CA356175778
NM_001145853.1:c.1513T>G