Canonical Allele Identifier: PA2741923573
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2654620
ClinVar RCV Id: RCV003439233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Leu521Arg
CA356175975
NM_006005.3:c.1562T>G