Canonical Allele Identifier: PA658812880
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 505398
ClinVar RCV Id: RCV000608372 RCV002529336 RCV003126844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Thr590Met
CA2839483
NM_006005.3:c.1769C>T