Canonical Allele Identifier: PA2825920152
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg517Cys
CA2839398
NM_001145853.1:c.1549C>T