Canonical Allele Identifier: PA324908
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215382
ClinVar RCV Id: RCV000200344 RCV000765776 RCV000767004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Glu273Lys
CA324907
NM_006005.3:c.817G>A