Canonical Allele Identifier: PA182629
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178596
ClinVar RCV Id: RCV000155346 RCV001155848 RCV001155849 RCV001510415 RCV003126557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala598Thr
CA182628
NM_006005.3:c.1792G>A