Canonical Allele Identifier: PA2825919885
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327580
ClinVar RCV Id: RCV001789842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Lys363Thr
CA356174225
NM_001145853.1:c.1088A>C