Canonical Allele Identifier: PA2825919891
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 349316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Asp367Asn
CA10618995
NM_001145853.1:c.1099G>A