Canonical Allele Identifier: PA319809
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Asp379Asn
CA319808
NM_006005.3:c.1135G>A