Canonical Allele Identifier: PA105683
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4521
ClinVar RCV Id: RCV000004779 RCV000726781 RCV001267554 RCV003155015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Leu829Pro
CA253199
NM_001145853.1:c.2486T>C