Canonical Allele Identifier: PA289141
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 130748
ClinVar RCV Id: RCV000118865 RCV000403034 RCV000336052 RCV000445373 RCV000987413 RCV000487646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg818Cys
CA289140
NM_006005.3:c.2452C>T