Canonical Allele Identifier: PA2825919403
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala48Val
CA136334
NM_001145853.1:c.143C>T