Canonical Allele Identifier: PA645395788
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Leu565Val
CA2839449
NM_006005.3:c.1693C>G