Canonical Allele Identifier: PA2499272367
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1071979
ClinVar RCV Id: RCV001384572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Arg629Trp
CA2839535
NM_006005.3:c.1885C>T