Canonical Allele Identifier: PA2825920594
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166605
ClinVar RCV Id: RCV000152694 RCV003147359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Phe775Val
CA179673
NM_001145853.1:c.2323T>G