Canonical Allele Identifier: PA105596
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92252
ClinVar RCV Id: RCV000077875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Glu462Gly
CA215002
NM_001145853.1:c.1385A>G