Canonical Allele Identifier: PA2825919958
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3061672
ClinVar RCV Id: RCV004544196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala406Asp
CA356174481
NM_001145853.1:c.1217C>A