Canonical Allele Identifier: PA2825919678
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Pro216Arg
CA2838986
NM_001145853.1:c.647C>G