Canonical Allele Identifier: PA2825920304
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala602Val
CA282578
NM_001145853.1:c.1805C>T