Canonical Allele Identifier: PA2825920207
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1348987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Glu550Ala
CA2839429
NM_001145853.1:c.1649A>C