Canonical Allele Identifier: PA1139720376
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 904987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Val580Glu
CA2839466
NM_006005.3:c.1739T>A