Canonical Allele Identifier: PA2825919870
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2110305
ClinVar RCV Id: RCV003042293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Tyr351Ser
CA356174154
NM_001145853.1:c.1052A>C