Canonical Allele Identifier: PA323936
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Asp339Asn
CA323935
NM_006005.3:c.1015G>A