Canonical Allele Identifier: PA2825920026
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 349318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Leu445Val
CA2839313
NM_001145853.1:c.1333C>G