Canonical Allele Identifier: PA2825919889
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Asp367Gly
CA2839218
NM_001145853.1:c.1100A>G