Canonical Allele Identifier: PA2825920501
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 137919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ile720Val
CA295580
NM_001145853.1:c.2158A>G