Canonical Allele Identifier: PA2825920341
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 289011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val624Ala
CA2839529
NM_001145853.1:c.1871T>C