Canonical Allele Identifier: PA2825920136
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1199553
ClinVar RCV Id: RCV001564250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val509Ile
CA356175823
NM_001145853.1:c.1525G>A