Canonical Allele Identifier: PA2825920216
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2418917
ClinVar RCV Id: RCV003112161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Leu554_Tyr563delinsHis
CA1058891765
NM_001145853.1:c.1661_1687del