Canonical Allele Identifier: PA129329
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30556
ClinVar RCV Id: RCV000023514 RCV000023515 RCV000200668 RCV000605882 RCV000623116 RCV001542531 RCV002280094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala684Val
CA129328
NM_006005.3:c.2051C>T