Canonical Allele Identifier: PA2825920192
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1351053
ClinVar RCV Id: RCV002051469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Cys541Arg
CA356176309
NM_001145853.1:c.1621T>C