Canonical Allele Identifier: PA645395695
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 252656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala57Thr
CA2838810
NM_006005.3:c.169G>A