Canonical Allele Identifier: PA2825920130
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328269
ClinVar RCV Id: RCV001795701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Pro504Arg
CA356175771
NM_001145853.1:c.1511C>G