Canonical Allele Identifier: PA2825920327
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala616Ser
CA2839519
NM_001145853.1:c.1846G>T