Canonical Allele Identifier: PA2825920108
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2181636
ClinVar RCV Id: RCV002606248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Gly494Cys
CA356175131
NM_001145853.1:c.1480G>T