Canonical Allele Identifier: PA1139720352
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 918063
ClinVar RCV Id: RCV001175317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Cys505Tyr
CA356175780
NM_006005.3:c.1514G>A