Canonical Allele Identifier: PA116904
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4526
ClinVar RCV Id: RCV000004784 RCV000020637 RCV000523215 RCV000599631 RCV001528145 RCV001544536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Glu864Lys
CA116903
NM_006005.3:c.2590G>A