Canonical Allele Identifier: PA2825920301
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val601Met
CA323280
NM_001145853.1:c.1801G>A