Canonical Allele Identifier: PA2825920200
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val545Met
CA320502
NM_001145853.1:c.1633G>A