Canonical Allele Identifier: PA916010219
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 805752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly45Arg
CA91787424
NM_006005.3:c.133G>A
CA356169701
NM_006005.3:c.133G>C