Canonical Allele Identifier: PA2825919998
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440151
ClinVar RCV Id: RCV001936810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Pro428Ala
CA356174602
NM_001145853.1:c.1282C>G