Canonical Allele Identifier: PA295790
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Glu385Lys
CA295789
NM_006005.3:c.1153G>A