Canonical Allele Identifier: PA2825920730
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 549512
ClinVar Variation Id: 591341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ser855Pro
CA2839780
NM_001145853.1:c.2563T>C
CA891862708
NM_001145853.1:c.2563_2565delinsCCG