Canonical Allele Identifier: PA2825920447
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440454
ClinVar RCV Id: RCV001978868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ile688Thr
CA91796801
NM_001145853.1:c.2063T>C