Canonical Allele Identifier: PA2573087712
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317613
ClinVar RCV Id: RCV001768179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Leu303Pro
CA356173863
NM_006005.3:c.908T>C