Canonical Allele Identifier: PA295581
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 137919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ile720Val
CA295580
NM_006005.3:c.2158A>G