Canonical Allele Identifier: PA2825919643
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1180254
ClinVar RCV Id: RCV001537423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Lys186Asn
CA356172029
NM_001145853.1:c.558G>C
CA356172030
NM_001145853.1:c.558G>T