Canonical Allele Identifier: PA2825920174
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2830264
ClinVar RCV Id: RCV003678686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Cys529Trp
CA2839413
NM_001145853.1:c.1587C>G