Canonical Allele Identifier: PA321853
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215394
ClinVar RCV Id: RCV000197395 RCV000825499 RCV000625904 RCV001175319 RCV001789765 RCV001375186 RCV002517281 RCV003884394 RCV004530182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly674Arg
CA321852
NM_006005.3:c.2020G>A
CA2839574
NM_006005.3:c.2020G>C