Canonical Allele Identifier: PA321921
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215357
ClinVar RCV Id: RCV001155752 RCV001155751 RCV001722099 RCV003126580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Val503Ile
CA321920
NM_006005.3:c.1507G>A