Canonical Allele Identifier: PA2825920157
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala519Val
CA295574
NM_001145853.1:c.1556C>T