Canonical Allele Identifier: PA645395702
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala126Thr
CA2838877
NM_006005.3:c.376G>A