Canonical Allele Identifier: PA105796
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45453
ClinVar RCV Id: RCV000404342 RCV000300529 RCV000515097 RCV000664095 RCV002464005 RCV002496613 RCV000038657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val779Met
CA282584
NM_001145853.1:c.2335G>A