Canonical Allele Identifier: PA2825920173
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317420
ClinVar RCV Id: RCV001767986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Tyr528Cys
CA356176108
NM_001145853.1:c.1583A>G