Canonical Allele Identifier: PA2825919780
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317613
ClinVar RCV Id: RCV001768179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Leu303Pro
CA356173863
NM_001145853.1:c.908T>C