Canonical Allele Identifier: PA323387
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215415
ClinVar RCV Id: RCV000198858 RCV002288801 RCV002492911 RCV004528985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ser888Leu
CA323386
NM_006005.3:c.2663C>T