Canonical Allele Identifier: PA282577
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45439
ClinVar RCV Id: RCV000038643 RCV000362526 RCV000307804 RCV000445534 RCV000755448 RCV002464003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly576Ser
CA282576
NM_006005.3:c.1726G>A