Canonical Allele Identifier: PA295583
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166608
ClinVar RCV Id: RCV000152697 RCV002056020 RCV003148661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ser790Trp
CA295582
NM_006005.3:c.2369C>G